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35368-57-1

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35368-57-1 Usage

Physical state

White to pale yellow solid

Usage

Organic synthesis, building block in pharmaceuticals and agrochemicals

Function

Intermediate in the synthesis of other compounds, antimicrobial and antifungal properties

Chemical structure

Benzene ring with a methyl group at the fourth carbon, acetamide group at the para position

Stability

Relatively stable and non-reactive

Toxicity

Low toxicity, not considered carcinogenic

Check Digit Verification of cas no

The CAS Registry Mumber 35368-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,6 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35368-57:
(7*3)+(6*5)+(5*3)+(4*6)+(3*8)+(2*5)+(1*7)=131
131 % 10 = 1
So 35368-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-7-2-4-8(5-3-7)12-6-9(10)11/h2-5H,6H2,1H3,(H2,10,11)

35368-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylphenoxy)acetamide

1.2 Other means of identification

Product number -
Other names p-Kresoxy-acetamid

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:35368-57-1 SDS

35368-57-1Relevant articles and documents

A phenoxy acetyl amine compound preparation method and phenoxy acetamide compounds

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Paragraph 0040; 0042; 0047; 0048; 0049-0053, (2019/05/21)

The invention belongs to the organic intermediates and the technical field of pharmaceutical intermediates, in particular to a phenoxy acetyl amine compound preparation method and phenoxy acetyl amine compound. The present invention provides a preparation method of the pervasive should be good, and green environmental protection, has better popularization and application value. The results show that the embodiment, the invention provides the above-mentioned method can prepare a plurality of phenoxy acetyl amine compound, and the yield can be 76%.

Aryloxyacetamidines and 2-(aryloxymethyl)-imidazolines.

Djerassi,Scholz

, p. 1688,1690 (2007/10/04)

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