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35628-00-3

  • Product Name:IPSDIENOL
  • Molecular Formula:C10H16O
  • Molecular Weight:152.236
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Product Details

Purity:99%

Factory supply IPSDIENOL 35628-00-3 with sufficient stock and high standard

  • Molecular Formula:C10H16O
  • Molecular Weight:152.236
  • Vapor Pressure:0.0103mmHg at 25°C 
  • Refractive Index:1.473 
  • Boiling Point:233.6 °C at 760 mmHg 
  • PKA:14?+-.0.20(Predicted) 
  • Flash Point:92.2 °C 
  • PSA：20.23000 
  • Density:0.87 g/cm3 
  • LogP:2.44580 

IPSDIENOL(Cas 35628-00-3) Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 48, p. 3122, 1983 DOI: 10.1021/jo00166a044Tetrahedron Letters, 26, p. 2797, 1985 DOI: 10.1016/S0040-4039(00)94915-3

InChI:InChI=1/C10H16O/c1-5-9(4)7-10(11)6-8(2)3/h5-6,10-11H,1,4,7H2,2-3H3/t10-/m1/s1

35628-00-3 Relevant articles

Enantioselective iridium-catalyzed carbonyl isoprenylation: Via alcohol-mediated hydrogen transfer

Xiang, Ming,Luo, Guoshun,Wang, Yuankai,Krische, Michael J.

, p. 981 - 984 (2019)

Highly enantioselective iridium catalyze...

Enantioselective synthesis of ipsenol and ipsdienol using a (2-bromoallyl)borane derivative

Yamamoto, Yasunori,Hara, Shoji,Suzuki, Akira

, p. 1029 - 1036 (1997)

(S)-(-)-Ipsenol and (S)-(+)-ipsdienol, a...

A new synthesis of the enantiomers of ipsdienol, the pheromone of the Ips bark beetles

Mori,Takikawa

, p. 2163 - 2168 (1991)

The enantiomers (~96% e.e.) of ipsdienol...

Improved synthesis of optically active ipsdienol

Kovalenko,Prokhorevich

, p. 757 - 758 (2016)

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Enantioselective Isoprenylboration Reaction of Aldehydes Catalyzed by a Chiral Phosphoric Acid

Zhang, Yu-Long,He, Bo-Jun,Xie, Yi-Wen,Wang, Yu-Hao,Wang, Yi-Long,Shen, Yong-Cun,Huang, Yi-Yong

supporting information, p. 3074 - 3079 (2019/05/15)

The BINOL-derived chiral phosphoric acid...

Stereoselective synthesis of (R)- and (S)-ipsdienols, pheromone components of bark beetles of the Ips family

Kovalenko,Matyushenkov

, p. 1168 - 1172 (2013/01/15)

Abstract-(R)- and (S)-Ipsdienols, compon...

35628-00-3 Process route

ipsdienol phthalate (1:1)

ipsdienol phthalate (1:1)

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35628-00-3

(4S)-2-methyl-6-methylideneocta-2,7-dien-4-ol

Conditions
Conditions Yield
With methanol; In tert-butyl alcohol; at 20 ℃; for 60h;
17.1 g
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134393-22-9

(S)-4-t-Butyldimethylsilyloxy-2-methyl-6-methyleneocta-2,7-diene

(4S)-2-methyl-6-methylideneocta-2,7-dien-4-ol
35628-00-3

(4S)-2-methyl-6-methylideneocta-2,7-dien-4-ol

Conditions
Conditions Yield
With tetrabutyl ammonium fluoride; In tetrahydrofuran; Ambient temperature;
92%

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