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6123-02-0

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6123-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6123-02-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6123-02:
(6*6)+(5*1)+(4*2)+(3*3)+(2*0)+(1*2)=60
60 % 10 = 0
So 6123-02-0 is a valid CAS Registry Number.

6123-02-0SDS

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 5-Chloromethyl-2-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-Chloromethyl-2-methoxybenzaldehyd

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:6123-02-0 SDS

6123-02-0Relevant articles and documents

Polysaccharides containing aromatic aldehydes and their derivatization via amine-aldehyde interactions

-

, (2008/06/13)

A polysaccharide derivative having the structure Sacch--O--Z--Ar--CH=N--Y or STR1 where Sacch--O-- represents a polysaccharide molecule; Z is --(CH2)n -- or STR2 Ar is a divalent aromatic group; Y is (a) a monovalent group derived fr

Transformation of Chloromethylbenzaldehydes into Corresponding (2-Nitroalkenyl-1) Benzyl Chlorides or Acetates. III

Grobelny, Damian,Witek, Stanislaw

, p. 536 - 542 (2007/10/02)

Unter den bekannten Methoden zur Darstellung von β-Nitrosostyrenen wurde der guenstigste Weg fuer die Synthese von (2-Nitroalk-1-enyl)-derivaten des Chlormethylbenzaldehydes 1 gesucht.Die besten Resultate erhaelt man durch Umsetzung der Aldehyde 1 a-c zu den Schiff'schen Basen 2 a-c und nachfolgende Kondensation der Verbindungen 2 a-c mit Nitroalkanen in Essigsaeure bei Raumtemperatur.Bei hoeheren Temperaturen liefern diese Umsetzungen die (2-Nitroalk-1-enyl)benzylacetate der Struktur 7-10.Die Struktur des Ausgangsaldehydes 1 bestimmt die Geschwindigkeit dieser Reakt ion.Ein moeglicher Mechanismus sowie die 1H-NMR-Spektren der erhaltenen Verbindungen werden diskutiert.

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