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1268265-90-2

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1268265-90-2 Usage

Abbreviation

ACBC

Type of compound

Cyclic amine and carbonitrile

Structure

Four-membered cyclobutane ring with an amino group and a cyano group attached

Usage

Organic synthesis as a building block for various compounds

Application

Pharmaceutical and agrochemical industries

Role

Can act as a ligand in coordination chemistry

Interaction

Forms complexes with transition metals

Potential use

Studied for its potential as a herbicide

Synthesis

Precursor for the synthesis of chiral compounds

Check Digit Verification of cas no

The CAS Registry Mumber 1268265-90-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,2,6 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1268265-90:
(9*1)+(8*2)+(7*6)+(6*8)+(5*2)+(4*6)+(3*5)+(2*9)+(1*0)=182
182 % 10 = 2
So 1268265-90-2 is a valid CAS Registry Number.

1268265-90-2SDS

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 N-[2-iodo-4-[2-(methylsulfamoyl)ethyl]phenyl]acetamide

1.2 Other means of identification

Product number -
Other names N-(2-Iodo-4-(2-(N-methylsulfamoyl)ethyl)phenyl)acetamide

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:1268265-90-2 SDS

1268265-90-2Relevant articles and documents

A PROCESS FOR THE SYNTHESIS OF NARATRIPTAN

-

, (2011/04/13)

The present invention relates to a process for preparing naratriptan or a salt thereof, the process comprising: (a) reacting a compound of formula (3) with a compound of the formula HCCR wherein Z is a protecting group, Y is a leaving group and R is a trialkyl silyl group, a trialkylstannyl group or a zinc (II) halide, to obtain the compound of formula (4); (b) converting the compound of formula (4) to a compound of formula (5) wherein Z'' is hydrogen or a benzyl group; (c) converting the compound of formula (5) to naratriptan; and (d) optionally converting naratriptan to a salt thereof. The present invention also provides novel compounds (3) and (4) and processes for their preparation.

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