Cas 132203-25-9,Phenylsulfanyl-acetic acid (R)-2-cyano-1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-ethyl ester

132203-25-9

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Basic information

Product Name: Phenylsulfanyl-acetic acid (R)-2-cyano-1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-ethyl ester
Synonyms:
CAS NO:132203-25-9
Molecular Formula:
Molecular Weight: 380.424
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: Phenylsulfanyl-acetic acid (R)-2-cyano-1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phenylsulfanyl-acetic acid (R)-2-cyano-1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-ethyl ester(132203-25-9)
EPA Substance Registry System: Phenylsulfanyl-acetic acid (R)-2-cyano-1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-ethyl ester(132203-25-9)

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: 132203-25-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132203-25-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,0 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132203-25:
(8*1)+(7*3)+(6*2)+(5*2)+(4*0)+(3*3)+(2*2)+(1*5)=69
69 % 10 = 9
So 132203-25-9 is a valid CAS Registry Number.

132203-25-9Upstream product

132155-84-1 (+/-)-N-<3-cyano-2-<(phenylthio)acetoxy>propyl>phthalimide

132203-25-9Downstream Products

132203-25-9Relevant academic research and scientific papers

Enhanced Enantioselectivity of an Enzymatic Reaction by the Sulfur Functional Group. A Simple Preparation of Optically Active β-Hydroxy Nitriles Using a Lipase

Itoh, Toshiyuki,Takagi, Yumiko,Nishiyama, Shigenori

, p. 1521 - 1524 (2007/10/02)

The enantioselectivity of a lipase-catalyzed hydrolysis was improved by varying the acyl residue into the sulfur functional one, i.e. the β-(phenylthio)- or β-(methylthio)acetoxy group, from acetate or valerate to realize satisfactory resolution of β-hydr

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