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3,5-DibroMo-1H-indazol-7-aMine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 316810-94-3 Structure
  • Basic information

    1. Product Name: 3,5-DibroMo-1H-indazol-7-aMine
    2. Synonyms: 3,5-DibroMo-1H-indazol-7-aMine
    3. CAS NO:316810-94-3
    4. Molecular Formula: C7H5Br2N3
    5. Molecular Weight: 290.9427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 316810-94-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-DibroMo-1H-indazol-7-aMine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-DibroMo-1H-indazol-7-aMine(316810-94-3)
    11. EPA Substance Registry System: 3,5-DibroMo-1H-indazol-7-aMine(316810-94-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 316810-94-3(Hazardous Substances Data)

316810-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 316810-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,8,1 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 316810-94:
(8*3)+(7*1)+(6*6)+(5*8)+(4*1)+(3*0)+(2*9)+(1*4)=133
133 % 10 = 3
So 316810-94-3 is a valid CAS Registry Number.

316810-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dibromo-2H-indazol-7-amine

1.2 Other means of identification

Product number -
Other names 3,5-Dibromo-1H-indazol-7-amine

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:316810-94-3 SDS

316810-94-3Downstream Products

316810-94-3Relevant articles and documents

Research in 7-aminoindazole series: Synthesis of new halo-7H-4-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-6-ones and 5H-9-halo-6-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-4-ones

Rakib,Benchidmi,Essassi,El Bouadili,Ibn Mansour,Bellan,Lopez,Lamande

, p. 339 - 345 (2007/10/03)

A new class of 7-aminohaloindazoles has been synthesized. Reactivity of the amino groups of these bicyclic systems has been investigated. The halogenated pyrazolo-1,5-benzodiazepinones have been synthesized by the condensation of 7-aminoindazoles with ethyl acetoacetate.

Reactivity of 7-aminoindazole as a bidendate nucleophile

Rakib, El Mostapha,Benchidmi, Mohammed,Essassi, El Mokhtar,Bouadili, Abdelaziz El,Khouili, Mostafa,Visseaux, Mark,Pujol, M.Dolors

, p. 2617 - 2627 (2007/10/03)

A simple route for the preparation of two new classes of heterocyclic systems: halopyrazolo[4,5-h]quinolines and halopyrazolo[1,5,4-ef][1,5]benzodiazepines, is presented. The effect of the solvent and the reactivity of pyrazolo-1,5-benzodiazepine were studied.

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