Cas 548786-21-6,(1S,2S)-cyclohex-4-ene-1,2-dicarboxylic acid diethyl ester

548786-21-6

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Basic information

Product Name: (1S,2S)-cyclohex-4-ene-1,2-dicarboxylic acid diethyl ester
Synonyms: (1S,2S)-cyclohex-4-ene-1,2-dicarboxylic acid diethyl ester
CAS NO:548786-21-6
Molecular Formula:
Molecular Weight: 226.273
EINECS: N/A
Product Categories: N/A
Mol File: 548786-21-6.mol
Article Data: 1

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,2S)-cyclohex-4-ene-1,2-dicarboxylic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S)-cyclohex-4-ene-1,2-dicarboxylic acid diethyl ester(548786-21-6)
EPA Substance Registry System: (1S,2S)-cyclohex-4-ene-1,2-dicarboxylic acid diethyl ester(548786-21-6)

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: 548786-21-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 548786-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,7,8 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 548786-21:
(8*5)+(7*4)+(6*8)+(5*7)+(4*8)+(3*6)+(2*2)+(1*1)=206
206 % 10 = 6
So 548786-21-6 is a valid CAS Registry Number.

548786-21-6Upstream product

548786-21-6Downstream Products

15679-28-4 ((1R,6R)-6-(hydroxymethyl)cyclohex-3-enyl)methanol

548786-21-6Relevant articles and documents

Triflimide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition

Ryu, Do Hyun,Corey

, p. 6388 - 6390 (2003)

The strong acid triflimide ((CF3SO2)2NH) protonates chiral oxazaborolidines to form superactive, stable, chiral Lewis acids which are highly effective catalysts for a wide variety of enantioselective Diels-Alder reactions, documented herein by more than 20 examples. Copyright

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