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15285-58-2

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15285-58-2 Usage

Uses

2-Hydroxy-4-azoniaspiro[3.5]nonane Chloride is used as a reagent in the synthesis of polyfunctional phosphorodithioates and its derivatives via nucleophilic ring opening of azetidinium ions. 2-Hydroxy-4-azoniaspiro[3.5]nonane Chloride is also a reagent in the synthesis of Arimoclomol Maleic Acid (A771270); an orally administered drug used to treat amyotrophic lateral sclerosis.

Check Digit Verification of cas no

The CAS Registry Mumber 15285-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15285-58:
(7*1)+(6*5)+(5*2)+(4*8)+(3*5)+(2*5)+(1*8)=112
112 % 10 = 2
So 15285-58-2 is a valid CAS Registry Number.

15285-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-pyrimidino-3-hydroxyazetidinium chloride

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-4-azoniaspiro[3.5]nonane

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:15285-58-2 SDS

15285-58-2Downstream Products

15285-58-2Relevant articles and documents

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Geartner,V.R.

, p. 523 - 530 (1968)

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Synthesis and pharmacological properties of new derivatives of 4-alkoxy-6-methyl-1h-pyrrolo[3,4-c]pyridine- 1,3(2h)-diones

Sladowska, Helena,Sabiniarz, Aleksandra,Sapa, Jacek,Filipek, Barbara

body text, p. 57 - 63 (2009/06/17)

Synthesis of 2-(2-hydroxy-3-amino)propyl derivatives of 4-alkoxy-6-methyl-1H-pyrrolo[3,4-c]pyridine-1,3(2H)-diones (24-35) is described. The chlorides used in the above synthesis exist mainly in the cyclic forms (18, 20-23). Only chloride with benzhydryl

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