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24886-73-5

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24886-73-5 Usage

Type of compound

Highly reactive organic azide

Structure

Rigid adamantane cage with an azide group attached

Common uses

a. Synthesis of various organic compounds
b. Production of energetic materials (explosives, propellants, pyrotechnics)
c. Precursor in organic synthesis for introducing azide functionality

Known for

Explosive nature

Safety precautions

Requires careful handling and storage to prevent accidents

Check Digit Verification of cas no

The CAS Registry Mumber 24886-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,8 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24886-73:
(7*2)+(6*4)+(5*8)+(4*8)+(3*6)+(2*7)+(1*3)=145
145 % 10 = 5
So 24886-73-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N3/c11-13-12-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2

24886-73-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Sigma-Aldrich

  • (276219)  1-Azidoadamantane  97%

  • 24886-73-5

  • 276219-1G

  • 489.06CNY

  • Detail
  • Sigma-Aldrich

  • (276219)  1-Azidoadamantane  97%

  • 24886-73-5

  • 276219-5G

  • 1,680.12CNY

  • Detail

24886-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Azidoadamantane

1.2 Other means of identification

Product number -
Other names 1-adamantyl azide

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:24886-73-5 SDS

24886-73-5Relevant articles and documents

Decarboxylative radical azidation using MPDOC and MM DOC esters

Nyfeler, Erich,Renaud, Philippe

supporting information; experimental part, p. 985 - 988 (2009/04/10)

An efficient radical-mediated decarboxylative azidation of aliphatic carboxylic acids has been developed. The success of this transformation hinges on the use of a new type of thiohydroxamate esters (MPDOC esters). These esters are more stable than the cl

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