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1538-87-0

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1538-87-0 Usage

Physical state

Colorless, flammable liquid

Odor

Sweet and strong

Chemical classification

Ether

Industrial uses

a. Solvent in pharmaceuticals
b. Solvent in pesticides
c. Solvent in fragrances

Application

Intermediate in the production of other chemicals

Reactivity

Highly reactive

Health hazards

a. Skin irritation
b. Eye irritation
c. Toxic if inhaled or ingested

Safety measures

Proper handling and storage procedures are essential

Check Digit Verification of cas no

The CAS Registry Mumber 1538-87-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1538-87:
(6*1)+(5*5)+(4*3)+(3*8)+(2*8)+(1*7)=90
90 % 10 = 0
So 1538-87-0 is a valid CAS Registry Number.

1538-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-1-methoxyethane

1.2 Other means of identification

Product number -
Other names 1-methoxyethyl-1-chloride

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:1538-87-0 SDS

1538-87-0Relevant articles and documents

The catalytic asymmetric acetalization

Kim, Ji Hye,Coric, Ilija,Vellalath, Sreekumar,List, Benjamin

supporting information, p. 4474 - 4477 (2013/05/21)

In straitened circumstances: In an asymmetric version of the acid-catalyzed acetalization of aldehydes, a novel member of the chiral confined Bronsted acid family significantly outperformed previously established catalysts, providing cyclic acetals with e

STUDY OF (1-ALKOXYETHYL)DIPHENYLPHOSPHINE OXIDES. I. SYNTHESES AND STRUCTURAL ANALYSES OF PHENYLETHOXY, METHOXY AND ISOPENTYLOXY DERIVATIVES

Ugliengo, Piero,Ahmed, Jamil,Viterbo, Davide,Calleri, Mariano,Ceruti, Maurizio

, p. 487 - 492 (2007/10/02)

1-Phenylethoxy- (9), 1-methoxy- (10), 1-isopentyloxy- (11) and 1-dodecyloxy- (12) ethyldiphenylphosphine oxides, key intermediates in the stereospecific syntheses of vinyl ethers, have been synthesised and characterised by 1H NMR and 13C NMR, IR and mass spectra.The crystal structures of compounds 9-11 have been determined by X-ray analysis.In the solid state only monomeric molecules have been found, despite the evidence of dimer formation in the mass spectra.The three molecules are in different conformations and a comparison with the geometry of similar compounds, retrieved from the Cambridge Structural Database, indicates a dominant contribution of the steric factors in dictating the different conformations.

Process for the preparation of N-α-alkoxyalkyl-carboxamides, and some representatives of this class of compounds and secondary products obtained therefrom

-

, (2008/06/13)

N-α-Alkoxyalkyl-carboxamides are prepared by reacting primary or secondary amides of aliphatic, araliphatic or aromatic carboxylic acids, or cyclic carboxamides (lactams) which are not capable of forming an aromatic system, with open-chain α-halogenoalkyl

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