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279682-92-7

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279682-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 279682-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,6,8 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 279682-92:
(8*2)+(7*7)+(6*9)+(5*6)+(4*8)+(3*2)+(2*9)+(1*2)=207
207 % 10 = 7
So 279682-92-7 is a valid CAS Registry Number.

279682-92-7 Well-known Company Product Price

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  • Sigma-Aldrich

  • (29245)  N1-[3,5-Bis(trifluoromethyl)benzyl]-N1-methylglycinamidehydrochloride  for GC derivatization, ≥99.0% (HPLC)

  • 279682-92-7

  • 29245-10MG-F

  • 389.61CNY

  • Detail
  • Sigma-Aldrich

  • (29245)  N1-[3,5-Bis(trifluoromethyl)benzyl]-N1-methylglycinamidehydrochloride  for GC derivatization, ≥99.0% (HPLC)

  • 279682-92-7

  • 29245-100MG-F

  • 2,331.81CNY

  • Detail

279682-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-N-[[3,5-bis(trifluoromethyl)phenyl]methyl]-N-methylacetamide,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-N-[3,5-bis(trifluoromethyl)benzyl]-N-methylacetamide hydrochloride

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:279682-92-7 SDS

279682-92-7Downstream Products

279682-92-7Relevant articles and documents

Detritylation with ytterbium triflate

Lu, Rong Jian,Liu, Daipei,Giese, Roger W.

, p. 2817 - 2819 (2000)

Ytterbium triflate catalyzes the hydrolysis of tritylamines and trityloxy compounds to the corresponding amines and alcohols under mild conditions in high yields. The reactions are conducted in tetrahydrofuran in the presence of 1 equivalent of water. (C) 2000 Elsevier Science Ltd.

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