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64075-36-1

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64075-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64075-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,7 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64075-36:
(7*6)+(6*4)+(5*0)+(4*7)+(3*5)+(2*3)+(1*6)=121
121 % 10 = 1
So 64075-36-1 is a valid CAS Registry Number.

64075-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-N-propylacetamide

1.2 Other means of identification

Product number -
Other names Phenyl-essigsaeure-propylamid

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:64075-36-1 SDS

64075-36-1Relevant articles and documents

Thoination of N-alkyl-O-acyl hydroxamic acid derivatives via Lawesson's reagent

Al-Faiyz, Yasair S.S.

, (2021/10/02)

N-alkyl-O-acyl thiohydroxamic acid derivatives were prepared in good yields by the treatment of their parent hydroxamic acids with Lawesson's reagent. Some of these thiohydroxamic acid derivatives exhibit the ability to undergo rearrangement under basic c

Method for synthesizing N-n-propylamide

-

Paragraph 0046-0050, (2019/04/04)

The invention belongs to the field of organic synthesis, and relates to a novel reaction method for selectively breaking a C-Nsigma bond in azacyclobutanamide and converting the bond into N-n-propylamide. According to the method, an azacyclobutanamide-bas

Catalyst-free amidation of aldehyde with amine under mild conditions

Yang, Hongyin,Hu, Wenjian,Deng, Shengjue,Wu, Tiantian,Cen, Haiman,Chen, Yiping,Zhang, Dela,Wang, Bo

supporting information, p. 5912 - 5915 (2015/08/11)

A highly efficient, catalyst-free and one-pot procedure for the direct synthesis of amides from aldehydes and amines under mild conditions has been developed. Both aliphatic and aromatic aldehydes with primary or secondary amines are successfully converted to the corresponding amides, and it is observed that reactions can proceed in either aqueous or organic media.

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