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212248-62-9

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  • High quality 1H-1-[(4-Aminophenyl)Methyl]-[1,2,4]-Triazole Dihydrochloride supplier in China

    Cas No: 212248-62-9

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212248-62-9 Usage

Uses

1-(4-Hydrazinylbenzyl)-1H-1,2,4-triazole can be used as an antimigraine drug.

Check Digit Verification of cas no

The CAS Registry Mumber 212248-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,2,4 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 212248-62:
(8*2)+(7*1)+(6*2)+(5*2)+(4*4)+(3*8)+(2*6)+(1*2)=99
99 % 10 = 9
So 212248-62-9 is a valid CAS Registry Number.

212248-62-9SDS

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 1-(4-Hydrazinophenyl)methyl-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 4-[1H-1,2,4-Triazole-1-YlMethyl]PhenylHydrazineHcl

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:212248-62-9 SDS

212248-62-9Relevant articles and documents

CONVERSION OF AROMATIC DIAZONIUM SALT TO ARYL HYDRAZINE

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Page/Page column 6-7, (2008/06/13)

The present invention relates to the preparation of aryl hydrazines and their salts by treating aryl diazonium salts with triphenyl phosphine followed by hydrolysis of the resulting triphenyl-aryl hydrazyl phosphonium salt to get aryl hydrazine or its sal

PROCESS FOR PREPARING RIZATRIPTAN

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Page 12-13; 15, (2008/06/13)

In particular, rizatriptan or a pharmaceutically acceptable salt thereof, which includes a) Preparation of the diazonium salt of the aniline hydrochloride (II); followed by reduction and acidification to give the hydrazine (III); b) reaction in situ of the hydrazine hydrochloride (III) with α-keto-δ-valerolactone, to give the hydrazone (IV); c) Fischer indole reaction of the hydrazone (IV), to give the pyranoindolone (V), optionally followed by a hydrolysis reaction to give (VI); d) Transesterification of (V) or esterification of its hydrolysis product (VI), to give (VII), where R means straight or branched C1-C4 alkyl chain; e) Conversion of the hydroxyl group of (VII) into dimethylamino, to give the indolecarboxylate (VIII), where R has the meaning defined above; f) Saponification of the 2-carboalkoxy group of (VIII) to give indolecarboxylic acid (IX); and g) Decarboxylation of the indolecarboxylic acid (IX) to give rizatriptan and, eventually, to obtain a pharmaceutically acceptable salt thereof. The invention also relates to synthesis intermediates to obtain rizatriptan.

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