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1497-83-2

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1497-83-2 Usage

Physical state

Colorless liquid

Boiling point

105-106 °C

Molecular weight

87.12 g/mol

Reactivity

Reactive intermediate

Applications

a. Synthesis of pharmaceuticals and agrochemicals
b. Monomer in polymer production
c. Crosslinking agent in adhesives and coatings

Toxicity

Highly toxic

Hazards

a. Skin irritation
b. Eye irritation
c. Respiratory system irritation

Safety precautions

Handle with care to avoid exposure

Check Digit Verification of cas no

The CAS Registry Mumber 1497-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1497-83:
(6*1)+(5*4)+(4*9)+(3*7)+(2*8)+(1*3)=102
102 % 10 = 2
So 1497-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO/c1-6-4-5-2-3-5/h2-4H2,1H3

1497-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(methoxymethyl)aziridine

1.2 Other means of identification

Product number -
Other names 1-methoxymethylaziridine

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:1497-83-2 SDS

1497-83-2Upstream product

1497-83-2Downstream Products

1497-83-2Relevant articles and documents

Structure of products of the reaction of 2-cyanoaziridine with carbonyl compounds

Koehler, K. F.,Zaddach, H.,Kadorkina, G. K.,Voznesenskii, V. N.,Chervin, I. I.,Kostyanovsky, R. G.

, p. 2049 - 2052 (1993)

The structure of azimexone (3), the product of the reaction of 2-cyanoaziridine with acetone, was confirmed on the basis of 1H and 13C NMR spectra.The formation of this product is accounted for by the α-aziridinoalkylating action of an intermediate containing a good leaving iminoyloxy group.Similar reactions were observed for 1-chloromethylaziridine and a 1-aziridinylmethylammonium salt (6), but not for 1-methoxymethylaziridine (7) and 1-aziridinemethanol. - Key words: 2-(2-cyanoaziridino)-2-(2-carbamoylaziridino)propane; 1-tert-butyl-2-carbamoylaziridine; α-1-aziridinoalkylation; 1H and 13C NMR spectra.

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