What is the 2-Methyl-L-proline Methyl ester hydrochloride?

2-Methyl-L-proline Methyl ester hydrochloride is , while it's Molecular Formula is C7H14ClNO2. Used in Pharmaceutical Research and Development: 2-Methyl-L-proline Methyl ester hydrochloride is used as a key component in the synthesis of peptides and proteins, contributing to the development of novel therapeutic agents and drug candidates. Its stability and ease of use in chemical synthesis make it an ideal candidate for creating complex organic molecules with potential medicinal properties. Used in Chemical Reactions as a Reagent: In the chemical industry, 2-Methyl-L-proline Methyl ester hydrochloride serves as a reagent in various chemical reactions, facilitating the formation of desired products and enhancing the efficiency of synthetic processes. Its solubility and reactivity make it a preferred choice for researchers and chemists working on the development of new chemical entities and materials. Used in Organic Synthesis as a Building Block: 2-Methyl-L-proline Methyl ester hydrochloride is utilized as a building block in organic synthesis, allowing for the construction of more complex organic molecules with specific functionalities and properties. Its presence in these molecules can influence their biological activity, making it a valuable tool in the design and synthesis of new compounds with potential applications in various fields, including medicine, agriculture, and materials science.

What is the CAS number for 2-Methyl-L-proline Methyl ester hydrochloride?

The CAS number of 2-Methyl-L-proline Methyl ester hydrochloride is 220060-08-2.

What is the 2-Methyl-L-proline Methyl ester hydrochloride?

2-Methyl-L-proline Methyl ester hydrochloride is , while it's Molecular Formula is C7H14ClNO2. Used in Pharmaceutical Research and Development: 2-Methyl-L-proline Methyl ester hydrochloride is used as a key component in the synthesis of peptides and proteins, contributing to the development of novel therapeutic agents and drug candidates. Its stability and ease of use in chemical synthesis make it an ideal candidate for creating complex organic molecules with potential medicinal properties. Used in Chemical Reactions as a Reagent: In the chemical industry, 2-Methyl-L-proline Methyl ester hydrochloride serves as a reagent in various chemical reactions, facilitating the formation of desired products and enhancing the efficiency of synthetic processes. Its solubility and reactivity make it a preferred choice for researchers and chemists working on the development of new chemical entities and materials. Used in Organic Synthesis as a Building Block: 2-Methyl-L-proline Methyl ester hydrochloride is utilized as a building block in organic synthesis, allowing for the construction of more complex organic molecules with specific functionalities and properties. Its presence in these molecules can influence their biological activity, making it a valuable tool in the design and synthesis of new compounds with potential applications in various fields, including medicine, agriculture, and materials science.

What is the CAS number for 2-Methyl-L-proline Methyl ester hydrochloride?

The CAS number of 2-Methyl-L-proline Methyl ester hydrochloride is 220060-08-2.

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220060-08-2

Q: What is 2-Methyl-L-proline Methyl ester hydrochloride (220060-08-2) used for?

2-Methyl-L-proline Methyl ester hydrochloride is a chemical compound derived from the amino acid proline, featuring a methyl ester group and a hydrochloride salt form. This derivative is characterized by its crystalline structure and high solubility in water, making it a stable and versatile building block in chemical synthesis and a valuable component in pharmaceutical research and development.

Product Name:2-Methyl-L-proline Methyl ester hydrochloride
Molecular Formula:C7H14ClNO2
Molecular Weight:179.64456

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Product Details

pd_meltingpoint:107-109 °C

Purity:99%

Manufacturer supply high quality 2-Methyl-L-proline Methyl ester hydrochloride 220060-08-2 with ISO standards

Molecular Formula:C7H14ClNO2
Molecular Weight:179.64456
Melting Point:107-109 °C
PSA：38.33000
LogP:1.43230

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220060-08-2 Process route

: 67-56-1
methanol

: 42856-71-3
(S)-2-methylpyrrolidine-2-carboxylic acid

: 220060-08-2,51098-46-5,1286768-32-8
methyl (S)-2-methylpyrrolidine-2-carboxylate monohydrochloride

Conditions

Conditions	Yield
With thionyl chloride; at 0 - 20 ℃; Inert atmosphere;	100%
With thionyl chloride; at -5 ℃; for 24h; Inert atmosphere; Reflux;	100%
With thionyl chloride; at 0 ℃; Reflux;	100%
With thionyl chloride; at 0 - 20 ℃;	85%
With hydrogenchloride; for 3h;
With thionyl chloride; at -5 ℃; for 24h; Inert atmosphere; Reflux;	0.62 mg
With thionyl chloride; for 3h;	1.1 g
With thionyl chloride; at 0 ℃; for 4.5h; Reflux;

: 220200-88-4
(3R,7aS)-7a-methyl-3-(trichloromethyl)tetrahydropyrrolo[1,2-c]oxazol-1(3H)-one

: 220060-08-2,51098-46-5,1286768-32-8
methyl (S)-2-methylpyrrolidine-2-carboxylate monohydrochloride

Conditions

Conditions	Yield
With thionyl chloride; at 0 - 20 ℃; for 0.333333h; Heating / reflux;	100%
With acetyl chloride; In methanol; for 4.5h; Reagent/catalyst; Inert atmosphere; Reflux;	48%

220060-08-2 Upstream products

67-56-1
methanol
220200-88-4
(3R,7aS)-7a-methyl-3-(trichloromethyl)tetrahydropyrrolo[1,2-c]oxazol-1(3H)-one
42856-71-3
(S)-2-methylpyrrolidine-2-carboxylic acid
118916-60-2
(2R,5S)-2-trichloromethyl-1-aza-3-oxabicyclo[3.3.0]octan-4-one

220060-08-2 Downstream products

220060-17-3
(S)-1-tert-butyl 2-methyl 2-methylpyrrolidine-1,2-dicarboxylate
853400-76-7
glycyl-L-2-methylprolyl-L-glutamic acid
1261569-85-0
(S)-8a-methyloctahydropyrrolo[1,2-a]pyrazine
1446261-55-7
(R)-methyl 11b-methyl-6-oxo-2,3,5,6,11,11b-hexahydro-1H-indolizino[8,7-b]indole-7-carboxylate

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