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4325-48-8

4325-48-8

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4325-48-8 Usage

Synthesis Reference(s)

Synthetic Communications, 26, p. 3479, 1996 DOI: 10.1080/00397919608003752

Check Digit Verification of cas no

The CAS Registry Mumber 4325-48-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4325-48:
(6*4)+(5*3)+(4*2)+(3*5)+(2*4)+(1*8)=78
78 % 10 = 8
So 4325-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H13Cl/c1-4-5-6(2,3)7/h4-5H2,1-3H3

4325-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-2-METHYLPENTANE

1.2 Other means of identification

Product number -
Other names Pentane,2-chloro-2-methyl

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:4325-48-8 SDS

4325-48-8Relevant articles and documents

Use of metal-accumulating plants for implementing chemical reactions

-

Page/Page column 38-40, (2015/10/28)

The use of metal-accumulating plants for implementing chemical reactions.

Free-radical transformations of di-tert-alkoxymethanes in the absence of solvent and in chloroform

Rol'nik, L. Z.,Kalashnikov, S. M.,Pastushenko, E. V.,Zlotskii, S. S.,Rakhmankulov, D. L.

, p. 614 - 618 (2007/10/02)

In chloroform in the presence of tert-butyl peroxide di-tert-alkoxymethanes from the corresponding tert-alkyl formates, tert-alkyl chlorides, and alkanes; here the chloroform is converted into methylene chloride and 1,1,2,2-tetrachloroethane.The relationships between the accumulation rate of the reaction products and the concentration of acetal, chloroform, and initiator were determined.An unbranched radical-chain mechanism was established for the fragmentation of the acetals with quadratic termination at the tert-alkyl and dichloromethyl radicals.

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