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4620-54-6

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4620-54-6 Usage

Physical form

Yellow solid

Molecular weight

215.29 g/mol

Class of compounds

Piperidinone compounds

Use in medicinal chemistry

Starting material for the synthesis of various pharmaceuticals and bioactive compounds

Pharmacological and biological activities

Potential role as a precursor in the synthesis of analgesic and local anesthetic drugs, potential role in the treatment of neurological disorders, and effects on the central nervous system

Importance

Diverse applications in the pharmaceutical and medical research fields

Check Digit Verification of cas no

The CAS Registry Mumber 4620-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,2 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4620-54:
(6*4)+(5*6)+(4*2)+(3*0)+(2*5)+(1*4)=76
76 % 10 = 6
So 4620-54-6 is a valid CAS Registry Number.

4620-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-piperidin-1-ylbut-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-piperidino-1-phenyl-2-buten-1-one

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:4620-54-6 SDS

4620-54-6Relevant articles and documents

STUDY OF THE ESCHENMOSER SULFIDE CONTRACTION METHOD WITH AND WITHOUT A THIOPHILE

Corsaro, A.,Perrini, G.,Testa, M. G.,Chiacchio, U.

, p. 197 - 206 (2007/10/02)

Results obtained and observations made by applying the title method for the synthesis of enaminones 5a-o, using triphenylphosphine as a thiophile and triethylamine as a base, are reported.The product distributions of the deprotonations of α-phenacylthio iminium bromides with and without thiophile and those known from thiouronium and heterocyclic thionium analogs are compared.Key words: Enaminones; α-phenacylthio iminium bromides; disulfides; thiiranes.

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