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112233-24-6

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  • 5,6-Dihydro-3-(methylamino)-2H-1,4-thiazin-2-one O-[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]oxime

    Cas No: 112233-24-6

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  • 2H-1,4-Thiazin-2-one, 5,6-dihydro-3-(methylamino)-, O-[[5-[(dimethylamino)methyl]-2-furanyl]methyl]oxime

    Cas No: 112233-24-6

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112233-24-6 Usage

Uses

Degradation product of Ranitidine (R120000)

Check Digit Verification of cas no

The CAS Registry Mumber 112233-24-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,3 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112233-24:
(8*1)+(7*1)+(6*2)+(5*2)+(4*3)+(3*3)+(2*2)+(1*4)=66
66 % 10 = 6
So 112233-24-6 is a valid CAS Registry Number.

112233-24-6SDS

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 (6Z)-6-[[5-[(dimethylamino)methyl]furan-2-yl]methoxyimino]-N-methyl-2,3-dihydro-1,4-thiazin-5-amine

1.2 Other means of identification

Product number -
Other names 5,6-Dihydro-3-(methylamino)-2H-1,4-thiazin-2-one O-[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]oxime

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112233-24-6 SDS

112233-24-6Upstream product

112233-24-6Downstream Products

112233-24-6Relevant articles and documents

Isolation and Identification of the Hydrolytic Degradation Products of Ranitidine Hydrochloride

Haywood, Phillip A.,Martin-Smith, Michael,Cholerton, Trevor J.,Evans, Michael B.

, p. 951 - 954 (2007/10/02)

Hydrolytic degradative studies on ranitidine hydrochloride (1) have shown that two different pathways are operative under strongly acid and strongly alkaline conditions.At intermediate pH values both pathways are operative whilst at very low pH values ranitidine hydrochloride is resistant to hydrolytic cleavage.This resistance to hydrolysis may be ascribed to C- protonation of the enediamine.

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