Cas 152377-33-8,2,2-Dimethyl-propionic acid 4-hydroxy-1-((Z)-4-trifluoromethanesulfonyloxy-but-3-enyl)-cyclohexa-2,5-dienylmethyl ester

152377-33-8

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Basic information

Product Name: 2,2-Dimethyl-propionic acid 4-hydroxy-1-((Z)-4-trifluoromethanesulfonyloxy-but-3-enyl)-cyclohexa-2,5-dienylmethyl ester
Synonyms: 2,2-Dimethyl-propionic acid 4-hydroxy-1-((Z)-4-trifluoromethanesulfonyloxy-but-3-enyl)-cyclohexa-2,5-dienylmethyl ester
CAS NO:152377-33-8
Molecular Formula:
Molecular Weight: 412.427
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: 2,2-Dimethyl-propionic acid 4-hydroxy-1-((Z)-4-trifluoromethanesulfonyloxy-but-3-enyl)-cyclohexa-2,5-dienylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-Dimethyl-propionic acid 4-hydroxy-1-((Z)-4-trifluoromethanesulfonyloxy-but-3-enyl)-cyclohexa-2,5-dienylmethyl ester(152377-33-8)
EPA Substance Registry System: 2,2-Dimethyl-propionic acid 4-hydroxy-1-((Z)-4-trifluoromethanesulfonyloxy-but-3-enyl)-cyclohexa-2,5-dienylmethyl ester(152377-33-8)

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: 152377-33-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 152377-33-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,3,7 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 152377-33:
(8*1)+(7*5)+(6*2)+(5*3)+(4*7)+(3*7)+(2*3)+(1*3)=128
128 % 10 = 8
So 152377-33-8 is a valid CAS Registry Number.

152377-33-8Upstream product

152377-33-8Downstream Products

152327-10-1 4-pivaloyloxymethyl-4-((Z)-4-trifluoromethanesulfonyloxy-3-butenyl)-2,5-cyclohexadien-1-one

152377-33-8Relevant academic research and scientific papers

Asymmetric Heck reaction: Catalytic asymmetric syntheses of bicyclic enones, dienones and the key intermediate for vernolepin

Kondo,Sodeoka,Mori,Shibasaki

, p. 920 - 930 (2007/10/02)

Bicyclic enone 23a, a functionalized decalin derivative, has been synthesized in up to 86% ee by an asymmetric Heck reaction starting with bisallylic alcohol 24. Enone 23a has been converted to 19, a key intermediate in the synthesis of vernolepin (14). F

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