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3,4,4-trimethylpentanamide is an organic compound with the molecular formula C9H19NO. It is a derivative of pentanamide, featuring three methyl groups attached to the carbon chain. The compound consists of a pentane backbone with three methyl groups at the 3rd, 4th, and 4th positions, and an amide functional group at the end. This amide group is formed by the condensation of a carboxylic acid and an amine, resulting in the release of a water molecule. 3,4,4-trimethylpentanamide is a colorless liquid with a low melting and boiling point, and it is soluble in organic solvents. It is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its amide functionality, it can also act as a chelating agent, forming complexes with metal ions.

7499-10-7

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7499-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7499-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7499-10:
(6*7)+(5*4)+(4*9)+(3*9)+(2*1)+(1*0)=127
127 % 10 = 7
So 7499-10-7 is a valid CAS Registry Number.

7499-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,4-trimethylpentanamide

1.2 Other means of identification

Product number -
Other names 3,4,4-Trimethyl-valeriansaeure-amid

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:7499-10-7 SDS

7499-10-7Downstream Products

7499-10-7Relevant articles and documents

tert-Butylation of α,β-unsaturated nitriles by tert-butylmercury halides in the presence of iodide ion

Russell, Glen A.,Chen, Ping,Yao,Kim

, p. 5967 - 5972 (2007/10/02)

Iodide ion promotes the free radical addition of t-BuHgI to acrylonitrile to form t-BuCH2CH(CN)HgI. A facile reaction of the adduct 1-cyanoalkyl radical with t-BuHgI2- is indicated. Further promotion is observed in the pre

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