What is the (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid?

(4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is , while it's Molecular Formula is C 16 H 18 N 2 O 2 S. Used in Pharmaceutical Industry: (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the dimethylamino substituted phenyl group and the 1,3-butadien-1-yl side chain, may contribute to its potential as a building block for developing new drugs with specific therapeutic properties. Used in Agrochemical Industry: In the agrochemical industry, (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid may be utilized as a component in the development of novel pesticides or herbicides. Its structural features could be exploited to target specific pests or weeds, offering an alternative to existing chemical solutions. Used in Materials Science: (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid can be employed in materials science for the creation of new materials with specialized properties. (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid's structure may allow for the development of materials with enhanced characteristics, such as improved stability, reactivity, or selectivity, depending on the application. Overall, the compound (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid holds promise in various scientific and industrial applications due to its unique structural features and potential for further research and development.

What is the CAS number for (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid?

The CAS number of (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is 1176235-08-7.

What is (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid (1176235-08-7) used for?

(4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is a complex organic compound that features a 4,5-dihydro-4-thiazolecarboxylic acid core, a 1,3-butadien-1-yl side chain, and a dimethylamino substituted phenyl group. It is part of the thiazole carboxylic acids and derivatives class, which are significant in various scientific fields due to their diverse applications.

What is the (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid?

(4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is , while it's Molecular Formula is C 16 H 18 N 2 O 2 S. Used in Pharmaceutical Industry: (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the dimethylamino substituted phenyl group and the 1,3-butadien-1-yl side chain, may contribute to its potential as a building block for developing new drugs with specific therapeutic properties. Used in Agrochemical Industry: In the agrochemical industry, (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid may be utilized as a component in the development of novel pesticides or herbicides. Its structural features could be exploited to target specific pests or weeds, offering an alternative to existing chemical solutions. Used in Materials Science: (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid can be employed in materials science for the creation of new materials with specialized properties. (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid's structure may allow for the development of materials with enhanced characteristics, such as improved stability, reactivity, or selectivity, depending on the application. Overall, the compound (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid holds promise in various scientific and industrial applications due to its unique structural features and potential for further research and development.

What is the CAS number for (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid?

The CAS number of (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is 1176235-08-7.

What is (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid (1176235-08-7) used for?

(4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid is a complex organic compound that features a 4,5-dihydro-4-thiazolecarboxylic acid core, a 1,3-butadien-1-yl side chain, and a dimethylamino substituted phenyl group. It is part of the thiazole carboxylic acids and derivatives class, which are significant in various scientific fields due to their diverse applications.

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1176235-08-7

Product Name:Aka Lumine
Molecular Weight:302.397

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Product Details

Purity:99%

Bulk supply high purity Aka Lumine 1176235-08-7, Paid sample available

Molecular Formula:C₁₆H₁₈N₂O₂S
Molecular Weight:302.397

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1176235-08-7 Process route

: 1176235-06-5
C₁₇H₂₀N₂O₂S

: 1176235-08-7
(4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid

Conditions

Conditions	Yield
With porcine liver esterase; ammonium bicarbonate; In ethanol; at 37 ℃; for 19h; pH=7.8; Inert atmosphere; Enzymatic reaction;	70 % ee

: 20432-35-3,6203-18-5
3-(4-dimethylamino-phenyl)-propenal

: 1176235-08-7
(4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]-1,3-butadien-1-yl]-4,5-dihydro-4-thiazolecarboxylic acid

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: toluene / 5 h / 20 °C 2: sodium hydroxide / isopropyl alcohol / 5 h / 20 °C 3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere 4: Triphenylphosphine oxide; trifluoromethylsulfonic anhydride / dichloromethane / 0.67 h / 20 °C / Inert atmosphere 5: porcine liver esterase; ammonium bicarbonate / ethanol / 19 h / 37 °C / pH 7.8 / Inert atmosphere; Enzymatic reaction With porcine liver esterase; dmap; trifluoromethylsulfonic anhydride; ammonium bicarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; Triphenylphosphine oxide; sodium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; toluene; 1: \|Wittig Olefination;

Yield

Multi-step reaction with 5 steps

1: toluene / 5 h / 20 °C

2: sodium hydroxide / isopropyl alcohol / 5 h / 20 °C

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

4: Triphenylphosphine oxide; trifluoromethylsulfonic anhydride / dichloromethane / 0.67 h / 20 °C / Inert atmosphere

5: porcine liver esterase; ammonium bicarbonate / ethanol / 19 h / 37 °C / pH 7.8 / Inert atmosphere; Enzymatic reaction

With porcine liver esterase; dmap; trifluoromethylsulfonic anhydride; ammonium bicarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; Triphenylphosphine oxide; sodium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; toluene; 1: |Wittig Olefination;

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