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124481-70-5

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124481-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124481-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,8 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 124481-70:
(8*1)+(7*2)+(6*4)+(5*4)+(4*8)+(3*1)+(2*7)+(1*0)=115
115 % 10 = 5
So 124481-70-5 is a valid CAS Registry Number.

124481-70-5SDS

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 dimethyl 2-(cyclohexylmethyl)pentanedioate

1.2 Other means of identification

Product number -
Other names Pentanedioic acid,2-(cyclohexylmethyl)-,dimethyl ester

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:124481-70-5 SDS

124481-70-5Downstream Products

124481-70-5Relevant articles and documents

A new approach for the generation and reaction of organotin hydrides: The development of reactions catalytic in tin

Terstiege, Ina,Maleczka Jr., Robert E.

, p. 342 - 343 (2007/10/03)

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Investigations on the Selectivity of the β-Scission of Alkyl-Radicals, II - Selectivity of the β-Fragmentation of α-(Methoxycarbonyl)alkyl Radicals

Metzger, Juergen O.,Klenke, Kurt

, p. 875 - 879 (2007/10/02)

The rate of β-scission of α-(methoxycarbonyl)alkyl radicals 3 and 9, generated by addition of cycloalkyl radicals to appropriate methyl 2-methylenealkanoates 1 and methyl (E)-2-alkenoates 8, resp., has been measured relative to the hydrogen transfer from cycloalkanes.The rate of β-scission increases with increasing stability of the leaving radical R*.Polar effects reversing the stability sequence have also been observed, e.g. the more stable (methoxycarbonyl)methyl radical leaves more slowly than a less stable secondary alkyl radical.

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