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39569-37-4

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39569-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39569-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,6 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39569-37:
(7*3)+(6*9)+(5*5)+(4*6)+(3*9)+(2*3)+(1*7)=164
164 % 10 = 4
So 39569-37-4 is a valid CAS Registry Number.

39569-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-acetylamino-phenyl)-ethanone oxime

1.2 Other means of identification

Product number -
Other names 3-Acetamino-acetophenon-oxim

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:39569-37-4 SDS

39569-37-4Relevant articles and documents

TETRAZOLINONE COMPOUND AND USE THEREOF

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Paragraph 0844-0845, (2015/11/16)

The compound represented by formula (1): wherein R4 and R5 each represents a hydrogen atom, a halogen atom, or a C1-C3 alkyl group; R6 represents a C1-C4 alkyl group, a C3-C6 cycloalkyl group, or the like; R7, R8, and R9 each represents a hydrogen atom, a halogen atom, or the like; R10 represents a C1-C3 alkyl group, or the like; R13 represents a C1-C3 alkyl group, or the like; and Q represents a phenyl group, or the like; has an excellent control effect on pests.

Synthesis of β-blocking oximes. Influence of terminal amine on β-selectivity

Amlaiky,Leclerc,Decker,Schwartz

, p. 437 - 439 (2007/10/02)

Three series of oximinopropanolamine derivatives in which the terminal nitrogen has been substituted by various arylalkyl groups were synthesized. The beta-adrenergic blocking activity of the 21 compounds was determined in vitro on the guinea-pig. The structure-activity relationship is discussed.

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