Cas 188563-10-2,4-[Benzyl-(2-chloro-acetyl)-amino]-cyclohex-1-enecarboxylic acid methyl ester

188563-10-2

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Basic information

Product Name: 4-[Benzyl-(2-chloro-acetyl)-amino]-cyclohex-1-enecarboxylic acid methyl ester
Synonyms: 4-[Benzyl-(2-chloro-acetyl)-amino]-cyclohex-1-enecarboxylic acid methyl ester
CAS NO:188563-10-2
Molecular Formula:
Molecular Weight: 321.804
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: 4-[Benzyl-(2-chloro-acetyl)-amino]-cyclohex-1-enecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-[Benzyl-(2-chloro-acetyl)-amino]-cyclohex-1-enecarboxylic acid methyl ester(188563-10-2)
EPA Substance Registry System: 4-[Benzyl-(2-chloro-acetyl)-amino]-cyclohex-1-enecarboxylic acid methyl ester(188563-10-2)

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: 188563-10-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 188563-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,5,6 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 188563-10:
(8*1)+(7*8)+(6*8)+(5*5)+(4*6)+(3*3)+(2*1)+(1*0)=172
172 % 10 = 2
So 188563-10-2 is a valid CAS Registry Number.

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188563-10-2Relevant academic research and scientific papers

Synthesis of 2-azabicyclo[3.3.1]lnonanes by means of (carbamoyl)dichloromethyl radical cyclization

Quirante, Josefina,Escolano, Carmen,Massot, Mireia,Bonjoch, Josep

, p. 1391 - 1402 (1997)

A new procedure for the synthesis of 2-azabicyclo[3.3.1]nonanes by intramolecular carboradical cyclization of 4-(trichloroacetamido)cyclohexenes substituted with an electron withdrawing substituent tester or nitrile) is described. The procedure allows the preparation of synthetically interesting azabicyclos 14 and 15 in nearly 70% yield.

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