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29945-90-2

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29945-90-2 Usage

Type of compound

Alkyne derivative

Chemical structure

Pent-4-ynamide group with two methyl substituents on the second carbon atom

Usage

Building block in organic synthesis and pharmaceutical research

Reactivity

Can undergo various reactions to produce different compounds with potential use in medicinal chemistry, materials science, and other fields

Value

Valuable tool in the development of new chemical compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 29945-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,4 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29945-90:
(7*2)+(6*9)+(5*9)+(4*4)+(3*5)+(2*9)+(1*0)=162
162 % 10 = 2
So 29945-90-2 is a valid CAS Registry Number.

29945-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethylpent-4-ynamide

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-4-pentynamide

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:29945-90-2 SDS

29945-90-2Downstream Products

29945-90-2Relevant articles and documents

-

Stevens,R.V. et al.

, p. 6637 - 6643 (1971)

-

Synthesis of Cyclic Enamides by Intramolecular Cyclization of Acetylenic Amides.

Jacobi, Peter A.,Brielmann, Harry L.,Hauck, Sheila I.

, p. 1193 - 1196 (2007/10/02)

Cyclic enamides 12 of a type useful in the synthesis of naturally occuring chlorins, isobacteriochlorins, and corrins have been prepared by a process involving Nicholas-Schreiber condensation to afford acetylenic amides 13, followed by either n-Bu4NF- or

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