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234-82-2

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234-82-2 Usage

Chemical Properties

Pale Yellow Solid

Uses

Different sources of media describe the Uses of 234-82-2 differently. You can refer to the following data:
1. Shows hypotensive action
2. Shows hypotensive action.

Check Digit Verification of cas no

The CAS Registry Mumber 234-82-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 234-82:
(5*2)+(4*3)+(3*4)+(2*8)+(1*2)=52
52 % 10 = 2
So 234-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H5N5/c1-2-4-7-6(3-1)5-9-13-8(7)10-11-12-13/h1-5H

234-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrazolo[5,1-a]phthalazine

1.2 Other means of identification

Product number -
Other names Tetrazolo[5,1-a]phthalazin

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:234-82-2 SDS

234-82-2Related news

Synthesis and positive inotropic evaluation of [1,2,4]triazolo[3,4-a]phthalazine and tetrazolo[5,1-a]phthalazine derivatives bearing substituted piperazine moieties09/29/2019

Four series of [1,2,4]triazolo[3,4-a]phthalazine and tetrazolo[5,1-a]phthalazine derivatives bearing substituted piperazine moieties were synthesized and evaluated for their positive inotropic activity by measuring the left atrium stroke volume in isolated rabbit-heart preparations. Several comp...detailed

Solid-phase synthesis of [1,2,4]triazolo[3,4-a]phthalazine and tetrazolo[5,1-a]phthalazine derivatives09/28/2019

A general method is reported for the solid-phase synthesis of [1,2,4]triazolo[3,4-a]phthalazine and tetrazolo[5,1-a]phthalazine derivatives based on the cyclization of resin-bound chlorophthalazines 4 with various hydrazides or sodium azide. The resin-bound chlorophthalazines 4, produced by nucl...detailed

234-82-2Relevant articles and documents

High-performance liquid chromatographic determination of nitrite ion by use of hydralazine

Noda,Minemoto,Noda,et al.

, p. 2541 - 2542 (1980)

-

SYNTHESIS OF 1,5-SUBSTITUTED TETRAZOLES FROM SECONDARY THIOAMIDES

Lehnhoff, Stefan,Ugi, Ivar

, p. 801 - 808 (2007/10/02)

A new, rather simple method for the conversion of thiamides and similar structures into 1,5-substituted tetrazoles is described.The procedure employs TMS-N3 and mild Lewis acid, like SnCl4 in an inert solvent at room temperature and leads to high yields.Such compounds are of increasing interest for their pharmaceutical properties.

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