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4-Chloro-3-methy-2-butenenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4450-34-4

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4450-34-4 Usage

Chemical Properties

Pale Yellow Oil

Uses

This item is a cis trans mixture.

Check Digit Verification of cas no

The CAS Registry Mumber 4450-34-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4450-34:
(6*4)+(5*4)+(4*5)+(3*0)+(2*3)+(1*4)=74
74 % 10 = 4
So 4450-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H6ClN/c1-5(4-6)2-3-7/h2H,4H2,1H3/b5-2+

4450-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-3-methylbut-2-enenitrile

1.2 Other means of identification

Product number -
Other names 4-CHLORO-3-METHYL-2-BUTENENITRILE

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:4450-34-4 SDS

4450-34-4Relevant academic research and scientific papers

Backbone modification of retinal induces protein-like excited state dynamics in solution

Sovdat, Tina,Bassolino, Giovanni,Liebel, Matz,Schnedermann, Christoph,Fletcher, Stephen P.,Kukura, Philipp

supporting information; experimental part, p. 8318 - 8320 (2012/06/30)

The drastically different reactivity of the retinal chromophore in solution compared to the protein environment is poorly understood. Here, we show that the addition of a methyl group to the C=C backbone of all-trans retinal protonated Schiff base acceler

Synthesis of 6H-Pyrrolotriazoles and 5H-Pyrrolotetrazoles: Alkylation and Acylation of the Monoanions

Dulcere, Jean-Pierre,Tawil, Mohamed,Santelli, Maurice

, p. 571 - 575 (2007/10/02)

Thermal cyclization of 1-azido-2-penten-4-ynes and 4-azido-2-butenenitriles led to 6H-pyrrolotriazoles and 5H-pyrrolotetrazoles, respectively, in good yields.Upon treatment with methyllithium these heterocyclic compounds gave the corr

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