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7-broMo-[1,2,3]triazolo[1,5-a]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107465-26-9 Structure
  • Basic information

    1. Product Name: 7-broMo-[1,2,3]triazolo[1,5-a]pyridine
    2. Synonyms: 7-broMo-[1,2,3]triazolo[1,5-a]pyridine
    3. CAS NO:107465-26-9
    4. Molecular Formula: C6H4BrN3
    5. Molecular Weight: 198.02006
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107465-26-9.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 7-broMo-[1,2,3]triazolo[1,5-a]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-broMo-[1,2,3]triazolo[1,5-a]pyridine(107465-26-9)
    11. EPA Substance Registry System: 7-broMo-[1,2,3]triazolo[1,5-a]pyridine(107465-26-9)
  • 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: 107465-26-9(Hazardous Substances Data)

107465-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107465-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,6 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107465-26:
(8*1)+(7*0)+(6*7)+(5*4)+(4*6)+(3*5)+(2*2)+(1*6)=119
119 % 10 = 9
So 107465-26-9 is a valid CAS Registry Number.

107465-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bromotriazolo[1,5-a]pyridine

1.2 Other means of identification

Product number -
Other names QC-8100

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:107465-26-9 SDS

107465-26-9Relevant articles and documents

Method for synthesizing [1,2,3]triazole[1,5-a]pyridines compound through non-catalyst N-N coupling reaction

-

Paragraph 0032-0037; 0048-0052; 0060-0062, (2019/04/04)

The invention relates to a method for synthesizing [1,2,3]triazole[1,5-a]pyridines compound through non-catalyst N-N coupling reaction. The invention discloses an efficient method for synthesizing a product at one step without using a catalyst under a mild condition from a 2-pyridylamine compound and nitroso tert-butyl ester as a mild nitrogen atom source. The method is free from the catalyst, thereaction step is reduced, the condition is extremely mild, the efficiency is high, and the later modification can be performed on the biological active molecular, thereby facilitating the industrialproduction of [1,2,3]triazole[1,5-a]pyridines compound.

Triazolopyridines. Part 7. Preparation of Bromo-triazolopyridines and-triazoloisoquinolines

Abarca, Belen,Ballesteros, Rafael,Mojarred, Fatemeh,Jones, Gurnos,Mouat, Deborah J.

, p. 1865 - 1868 (2007/10/02)

Bromination of the 7-lithiotriazolopyridines (7) and (10) gave small yields of the 7-bromotriazolopyridines (8) and (11).Some ring opening was observed with the lithium derivative (7); ring opening was a major reaction when bromine reacted with 5-lithiotriazoloisoquinoline (15) or with the 7-trimethylsilyltriazolopyridine (20).Good yields of 7-bromotriazolopyridines (8) and (18) and of 5-bromotriazoloisoquinoline (19) were obtained from the appropriate lithio derivative and dibromotetrachloroethane.The properties of 5-trimethylsilyltriazoloisoquinoline and its lithium derivative are reported; protodesilylation has been achieved with compounds (25)-(28).

NUCLEOPHILIC SUBSTITUTIONS ON BROMOTRIAZOLOPYRIDINES - AN IMPROVED ROUTE TO 2,6-DISUBSTITUTED PYRIDINES AND TO 1,3-DISUBSTITUTED ISOQUINOLINES

Abarca, Belen,Ballesteros, Rafael,Jones, Gurnos,Mojarrad, Fatemeh

, p. 3543 - 3546 (2007/10/02)

A regiospecific synthesis of 2,6-disubstituted pyridines and of 1,3-disubstituted isoquinolines is described.

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