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3-Methyl-2-butenal dimethyl hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16713-48-7

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16713-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16713-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,1 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16713-48:
(7*1)+(6*6)+(5*7)+(4*1)+(3*3)+(2*4)+(1*8)=107
107 % 10 = 7
So 16713-48-7 is a valid CAS Registry Number.

16713-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-butenal dimethylhydrazone

1.2 Other means of identification

Product number -
Other names 3-Methyl-but-2-enal-N,N-dimethyl-hydrazon

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:16713-48-7 SDS

16713-48-7Relevant academic research and scientific papers

α-Alkylation of α,β-Unsaturated Aldehyde Dimethylhydrazones Accompanied with the Double Bond Migration to β,γ

Yamashita, Masakazu,Matsumiya, Kaoru,Nakano, Ken-ichi

, p. 1759 - 1763 (2007/10/02)

Lithiated α,β-unsaturated aldehyde N,N-dimethylhydrazones reacted with alkyl halides accompanied by double bond migration to give α-alkylated β,γ-unsaturated aldehyde N,N-dimethylhydrazones in satisfactory yields.This reaction was found to be caused at the first step by deprotonation from a γ-carbon atom by lithium diisopropylamide.In the case of hydrazones with two kinds of γ-protons, deprotonation from the less hindered γ-carbon occurred selectively.Using this reaction, a novel sesquiterpene, 2,5,9-trimethyl-2-vinyl-4,8-decadienal, which has a vinyl group at the α-position, was synthesized in a good yield.

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