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930-66-5

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930-66-5 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 101, p. 228, 1979 DOI: 10.1021/ja00495a043

Check Digit Verification of cas no

The CAS Registry Mumber 930-66-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 930-66:
(5*9)+(4*3)+(3*0)+(2*6)+(1*6)=75
75 % 10 = 5
So 930-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H9Cl/c7-6-4-2-1-3-5-6/h4H,1-3,5H2

930-66-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chlorocyclohexene

1.2 Other means of identification

Product number -
Other names 1-chlorocyclohex-1-ene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:930-66-5 SDS

930-66-5Relevant articles and documents

Cyclohexeno[3,4]cyclodec-1,5-diyne-3-ene: A Convenient Enediyne

Perrin, Charles L.,Shrinidhi, Annadka

supporting information, p. 6911 - 6915 (2021/09/14)

Enediynes are widely studied to understand their cycloaromatization and the trapping of the resulting p-dehydrobenzene diradical. However, few model substrates are known, and they are hard to synthesize and difficult to handle. Herein we report cyclohexen

Synthesis of Vinyl Chlorides via Triphosgene-Pyridine Activation of Ketones

Saputra, Mirza A.,Ngo, Ly,Kartika, Rendy

, p. 8815 - 8820 (2015/09/15)

Herein, we describe a mild method to prepare aliphatic and aromatic vinyl chlorides from their corresponding ketones via triphosgene-pyridine activation in dichloromethane at reflux. The mechanism of this reaction is proposed to involve formation of a put

Structure and Dynamic Features of an Intramolecular Frustrated Lewis Pair

Axenov, Kirill V.,Moemming, Cornelia M.,Kehr, Gerald,Froehlich, Roland,Erker, Gerhard

supporting information; experimental part, p. 14069 - 14073 (2011/02/23)

Di(mesityl)cyclohexenylphosphine undergoes hydroboration with Piers' borane [HB(C6F5)2] to yield the cyclohexylene- anellated frustrated Lewis pair 5. This P/B pair splits H2 with the formation of the product 4

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