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256507-84-3

256507-84-3

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256507-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 256507-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,5,0 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 256507-84:
(8*2)+(7*5)+(6*6)+(5*5)+(4*0)+(3*7)+(2*8)+(1*4)=153
153 % 10 = 3
So 256507-84-3 is a valid CAS Registry Number.

256507-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-(N-propanoylanilino)piperidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-benzyl-4-[phenyl(propionyl)amino]piperidine-4-carboxylic acid

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:256507-84-3 SDS

256507-84-3Relevant articles and documents

OPIOID HAPTENS, CONJUGATES, VACCINES, AND METHODS OF GENERATING ANTIBODIES

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Paragraph 0259-0260, (2020/02/14)

The disclosure provides, inter alia, opioid haptens, opioid hapten conjugates, opioid vaccines, methods of treating or preventing opioid use disorder, methods of treating opioid overdose, and methods of generating and/or isolating antibodies selective for opioids.

A convenient method for the N-acylation and esterification of hindered amino acids: Synthesis of ultra short acting opioid agonist, remifentanil

Coleman, Mark J.,Goodyear, Michael D.,Latham, David W. S.,Whitehead, Andrew J.

, p. 1923 - 1924 (2007/10/03)

A general method has been devised for the one step preparation of N- acylamino acid esters of type 7 from the corresponding a-amino acids in high yield under mild conditions and a probable mechanism is proposed.