Cas 191406-52-7,(2R,3S)-3-Phenyl-2-phenylsulfanyl-pent-4-enoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

191406-52-7

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Basic information

Product Name: (2R,3S)-3-Phenyl-2-phenylsulfanyl-pent-4-enoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms:
CAS NO:191406-52-7
Molecular Formula:
Molecular Weight: 422.632
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3S)-3-Phenyl-2-phenylsulfanyl-pent-4-enoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-3-Phenyl-2-phenylsulfanyl-pent-4-enoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(191406-52-7)
EPA Substance Registry System: (2R,3S)-3-Phenyl-2-phenylsulfanyl-pent-4-enoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(191406-52-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 191406-52-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 191406-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,4,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 191406-52:
(8*1)+(7*9)+(6*1)+(5*4)+(4*0)+(3*6)+(2*5)+(1*2)=127
127 % 10 = 7
So 191406-52-7 is a valid CAS Registry Number.

191406-52-7Upstream product

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191406-52-7Relevant academic research and scientific papers

Co(III)-salen catalyzed carbenoid reaction: Stereoselective [2,3]sigmatropic rearrangement of S-ylides derived from allyl aryl sulfides

Fukuda, Tsutomu,Katsuki, Tsutomu

, p. 3435 - 3438 (1997)

Allyl aryl sulfides and diazoacetic acid esters react in the presence of optically active Co(III)-salen complex (4) with good enantioselectivity, to give the [2,3]sigmatropic rearrangement products, 2-arylthio-3-aryl-4-pentenoic acid esters, via the corresponding S-ylides.

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