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41864-24-8

41864-24-8

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41864-24-8 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 41864-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,6 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41864-24:
(7*4)+(6*1)+(5*8)+(4*6)+(3*4)+(2*2)+(1*4)=118
118 % 10 = 8
So 41864-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H11N3O2/c1-7(2,3)12-6(11)10-5-8-4-9-10/h4-5H,1-3H3

41864-24-8 Well-known Company Product Price

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  • TCI America

  • (B1969)  1-tert-Butoxycarbonyl-1,2,4-triazole  >97.0%(GC)

  • 41864-24-8

  • 5g

  • 790.00CNY

  • Detail

  • TCI America

  • (B1969)  1-tert-Butoxycarbonyl-1,2,4-triazole  >97.0%(GC)

  • 41864-24-8

  • 25g

  • 2,450.00CNY

  • Detail

41864-24-8SDS

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 tert-butyl 1,2,4-triazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-tert-Butoxycarbonyl-1,2,4-triazole

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:41864-24-8 SDS

41864-24-8Downstream Products

41864-24-8Relevant articles and documents

An efficient and chemoselective Br?nsted acidic ionic liquid-catalyzed N-Boc protection of amines

Sunitha, Sadula,Kanjilal, Sanjit,Reddy, P. Srinivasa,Prasad, Rachapudi B.N.

, p. 2527 - 2532 (2008/09/19)

The first report of a Br?nsted acidic ionic liquid, 1-methylimidazolium tetrafluoroborate [(HMIm)BF4], catalyzed efficient and chemoselective N-Boc protection of various amines using (Boc)2O is presented. Optically pure amino alcohols and amino acid esters were converted efficiently to their corresponding optically pure N-Boc derivatives. The reported method is mild, solvent-free and has the advantages of both homogeneous and heterogeneous catalysis with high product yields, selectivity and ease of product separation.

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