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37101-10-3

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37101-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37101-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37101-10:
(7*3)+(6*7)+(5*1)+(4*0)+(3*1)+(2*1)+(1*0)=73
73 % 10 = 3
So 37101-10-3 is a valid CAS Registry Number.

37101-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyiminopropanenitrile

1.2 Other means of identification

Product number -
Other names 2-Hydroxyximinopropionitril

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:37101-10-3 SDS

37101-10-3Relevant articles and documents

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Kissinger,L.W.,Ungnade,H.E.

, p. 1471 - 1473 (1960)

-

Synthesis and reactivity of furazanyl- and furoxanyldiazonium salts

Rakitin, O. A.,Zalesova, O. A.,Kulikov, A. S.,Makhova, N. N.,Godovikova, T. I.,Khmel'nitskii, L. I.

, p. 1865 - 1870 (2007/10/02)

Diazotization of aminofurazans (1) and 4-aminofuroxans (2) with nitrosylsulfuric acid in a mixture of conc.H2SO4 and H3PO4 has been studied and offered as a general method for preparing furazanyl- (3) and furoxanyldiazonium (4) salts.It has been shown tha

INVESTIGATION OF THE MECHANISM OF FORMATION OF HETEROCYCLES BY NMR SPECTROSCOPY. V. 3-AMINO-4-METHYLFURAZAN

Vergizov, S. N.,Selivanov, S. I.,Mel'nikova, S. F.,Ershov, B. A.,Tselinskii, I. V.

, p. 374 - 377 (2007/10/02)

The kinetics of the reaction of hydroxyiminoacetone with hydroxylamine were studied by PMR spectroscopy.The formation of 3-amino-4-methylfurazan is a multistage process; the intermediate products are methylglyoxime, methylfurazan, α-hydroxyiminopropionitrile, and methylaminoglyoxime, and the side product is α-hydroxyiminopropionamide.

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