Cas 879292-74-7,(1S,2R)-thioacetic acid S-[3-benzyloxy-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-trifluoromethyl-propyl] ester

879292-74-7

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Basic information

Product Name: (1S,2R)-thioacetic acid S-[3-benzyloxy-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-trifluoromethyl-propyl] ester
Synonyms:
CAS NO:879292-74-7
Molecular Formula:
Molecular Weight: 437.439
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: (1S,2R)-thioacetic acid S-[3-benzyloxy-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-trifluoromethyl-propyl] ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R)-thioacetic acid S-[3-benzyloxy-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-trifluoromethyl-propyl] ester(879292-74-7)
EPA Substance Registry System: (1S,2R)-thioacetic acid S-[3-benzyloxy-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-trifluoromethyl-propyl] ester(879292-74-7)

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: 879292-74-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 879292-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,2,9 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 879292-74:
(8*8)+(7*7)+(6*9)+(5*2)+(4*9)+(3*2)+(2*7)+(1*4)=237
237 % 10 = 7
So 879292-74-7 is a valid CAS Registry Number.

879292-74-7Upstream product

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879292-74-7Relevant academic research and scientific papers

Asymmetric synthesis of both enantiomers of syn-(3-trifluoromethyl)cysteine derivatives

Jiang, Zhong-Xing,Liu, Xiao-Ping,Qiu, Xiao-Long,Qing, Feng-Ling

, p. 499 - 505 (2005)

The use of several chiral trifluoromethylated building blocks 1a, 1b, 9a and 9b was attempted to synthesize of syn-(3-trifluoromethyl)cysteine. A novel and efficient enantioselective synthesis of both enantiomers of syn-(3-trifluoromethyl)cysteine derivat

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