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753452-41-4

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753452-41-4 Usage

Physical State

Colorless to pale yellow liquid

Odor

Pungent

Solubility

Soluble in water and ethanol

Common Uses

Production of polymers and resins
Specialty chemical in adhesives, coatings, and sealants manufacturing

Hazards

Hazardous if ingested, inhaled, or in contact with skin

Safety Precautions

Handle with care
Proper safety measures should be observed when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 753452-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,3,4,5 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 753452-41:
(8*7)+(7*5)+(6*3)+(5*4)+(4*5)+(3*2)+(2*4)+(1*1)=164
164 % 10 = 4
So 753452-41-4 is a valid CAS Registry Number.

753452-41-4SDS

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 N-(1-Methyl-cyclopent-3-enyl)-acrylamide

1.2 Other means of identification

Product number -
Other names -

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:753452-41-4 SDS

753452-41-4Downstream Products

753452-41-4Relevant articles and documents

Double ring-closing metathesis reaction of nitrogen-containing tetraenes: Efficient construction of bicyclic alkaloid skeletons and synthetic application to four stereoisomers of lupinine and their derivatives

Ma, Shengming,Ni, Bukuo

, p. 3286 - 3300 (2007/10/03)

The double ring-closing metathesis reaction of nitrogen-containing tetraenes was studied. The selectivity of the fused/dumbbell-type products can be controlled by the electronic/steric effects of the substituents attached to the C=C bonds and the s-cis/s-trans conformational ratios of the substrates. This methodology has also been successfully applied to the enantioselective synthesis of four stereoisomers of lupinine and their derivatives.

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