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57152-87-1

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57152-87-1 Usage

General Description

1-Chloro-10-iododecane is a chemical compound with the molecular formula C12H24ClI. It is a long-chain alkyl iodide with a chloro substituent on the first carbon atom. 1-chloro-10-iododecane is often used as a reagent in organic synthesis, particularly in the preparation of alkyl iodides. It has also been investigated for its potential applications in the field of organic electronics and as a precursor for the synthesis of various organic compounds. 1-Chloro-10-iododecane is considered to be a hazardous chemical and should be handled with care due to its potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 57152-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,5 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57152-87:
(7*5)+(6*7)+(5*1)+(4*5)+(3*2)+(2*8)+(1*7)=131
131 % 10 = 1
So 57152-87-1 is a valid CAS Registry Number.

57152-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-10-iododecane

1.2 Other means of identification

Product number -
Other names 1-Chlor-10-iod-decan

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:57152-87-1 SDS

57152-87-1Relevant articles and documents

Photon can tremendously accelerate the alkyl iodides' elimination in water

Liu, Wenbo,Li, Chao-Jun

supporting information, p. 1699 - 1702 (2015/03/14)

Elimination of the alkyl halides in water is very difficult due to the heterogeneous nature and the limitation of base strength. We discovered that ultra-violet (UV) light can enhance the elimination rate of alkyl iodides, including primary, secondary, and tertiary iodides in water dramatically for the first time. We propose a tandem radical-carbocation reaction mechanism to rationalize this special property of alkyl iodides.

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