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3-Buten-2-one, 3-(4-chlorophenyl)-1-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

872891-63-9

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872891-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872891-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,8,9 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 872891-63:
(8*8)+(7*7)+(6*2)+(5*8)+(4*9)+(3*1)+(2*6)+(1*3)=219
219 % 10 = 9
So 872891-63-9 is a valid CAS Registry Number.

872891-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenyl)-1-hydroxybut-3-en-2-one

1.2 Other means of identification

Product number -
Other names 3-Buten-2-one,3-(4-chlorophenyl)-1-hydroxy

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:872891-63-9 SDS

872891-63-9Upstream product

872891-63-9Downstream Products

872891-63-9Relevant academic research and scientific papers

Chemistry of 1,2,4-trioxanes: Base-mediated formation of highly reactive electrophiles and their entrapment with amines and thiols

Singh, Chandan,Malik, Heetika

, p. 3485 - 3489 (2008/02/10)

6-(1-Arylvinyl)-substituted 1,2,4-trioxanes undergo a highly facile fragmentation under mild basic conditions to furnish 3-aryl-1-hydroxybut-3-en-2- ones, which react very efficiently with various amines and thiols to give Michael adducts. Both the formation of the reactive 3-aryl-1-hydroxybut-3-en-2- ones and their subsequent reaction with amines and thiols can be achieved in one pot. Georg Thieme Verlag Stuttgart.

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