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Benzene, (1-chlorocyclopropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116005-40-4

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116005-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116005-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,0 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116005-40:
(8*1)+(7*1)+(6*6)+(5*0)+(4*0)+(3*5)+(2*4)+(1*0)=74
74 % 10 = 4
So 116005-40-4 is a valid CAS Registry Number.

116005-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-chlorocyclopropyl)benzene

1.2 Other means of identification

Product number -
Other names 1-phenylchlorocyclopropane

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:116005-40-4 SDS

116005-40-4Downstream Products

116005-40-4Relevant academic research and scientific papers

Access to cyclopropyl cations via carbene fragmentation

Moss, Robert A.,Chu, Gaosheng

, p. 3321 - 3326 (2007/10/03)

Photolysis of cyclopropyloxychlorodiazirines affords cyclopropyloxychlorocarbenes whose fragmentations provide access to ion pairs, which feature cyclopropyl cations.

FREE RADICAL CHLORINATION AND ONE-ELECTRON OXIDATION OF ARYLCYCLOPROPANES. DESIGNER PROBES FOR CYTOCHROME P-450 HYDROXYLATION MECHANISMS

Riley, Pamela,Hanzlik, Robert P.

, p. 3015 - 3018 (2007/10/02)

Arylcyclopropyl radicals can be formed under mild conditions (phase-transfer-catalyzed chlorination) and give rise to cyclopropyl products; in contrast one-electron oxidation of arylcyclopropanes by Mn(OAc)3 leads to fragmentation of the cyclopropane ring and the formation of acyclic products.

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