Cas 1372800-84-4,(1R,2R,6R)-triethyl 1-cyano-6-(naphthalen-2-yl)cyclohex-3-ene-1,2,3-tricarboxylate

1372800-84-4

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Basic information

Product Name: (1R,2R,6R)-triethyl 1-cyano-6-(naphthalen-2-yl)cyclohex-3-ene-1,2,3-tricarboxylate
Synonyms: (1R,2R,6R)-triethyl 1-cyano-6-(naphthalen-2-yl)cyclohex-3-ene-1,2,3-tricarboxylate
CAS NO:1372800-84-4
Molecular Formula:
Molecular Weight: 449.503
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: (1R,2R,6R)-triethyl 1-cyano-6-(naphthalen-2-yl)cyclohex-3-ene-1,2,3-tricarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,6R)-triethyl 1-cyano-6-(naphthalen-2-yl)cyclohex-3-ene-1,2,3-tricarboxylate(1372800-84-4)
EPA Substance Registry System: (1R,2R,6R)-triethyl 1-cyano-6-(naphthalen-2-yl)cyclohex-3-ene-1,2,3-tricarboxylate(1372800-84-4)

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: 1372800-84-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1372800-84-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,8,0 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1372800-84:
(9*1)+(8*3)+(7*7)+(6*2)+(5*8)+(4*0)+(3*0)+(2*8)+(1*4)=154
154 % 10 = 4
So 1372800-84-4 is a valid CAS Registry Number.

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1372800-84-4Relevant academic research and scientific papers

Highly enantioselective [4 + 2] cycloadditions of allenoates and dual activated olefins catalyzed by N-acyl aminophosphines

Xiao, Hua,Chai, Zhuo,Cao, Dongdong,Wang, Hongyu,Chen, Jinghao,Zhao, Gang

experimental part, p. 3195 - 3201 (2012/06/01)

An asymmetric organocatalytic [4 + 2] cycloaddition between α-substituted allenoates and dual activated olefins using bifunctional N-acyl aminophosphine catalysts is described. The use of 2-cyano acrylate derived olefins led to the first successful incorp

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