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166881-42-1

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166881-42-1 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 166881-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,8,8 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 166881-42:
(8*1)+(7*6)+(6*6)+(5*8)+(4*8)+(3*1)+(2*4)+(1*2)=171
171 % 10 = 1
So 166881-42-1 is a valid CAS Registry Number.

166881-42-1 Well-known Company Product Price

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  • Aldrich

  • (689459)  Fmoc-N-(2,4-dimethoxybenzyl)-Gly-OH  ≥98.0% (HPLC)

  • 166881-42-1

  • 689459-250MG

  • 1,346.67CNY

  • Detail
  • Aldrich

  • (689459)  Fmoc-N-(2,4-dimethoxybenzyl)-Gly-OH  ≥98.0% (HPLC)

  • 166881-42-1

  • 689459-1G

  • 4,298.58CNY

  • Detail

166881-42-1SDS

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 2-[(2,4-dimethoxyphenyl)methyl-(9H-fluoren-9-ylmethoxycarbonyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names Fmoc-N-(2,4-dimethoxybenzyl)-Gly-OH

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:166881-42-1 SDS

166881-42-1Relevant articles and documents

A combined solid- and solution-phase approach provides convenient access to analogues of the calcium-dependent lipopeptide antibiotics

Hart, Peter 'T,Kleijn, Laurens H. J.,De Bruin, Gerjan,Oppedijk, Sabine F.,Kemmink, Johan,Martin, Nathaniel I.

, p. 913 - 918 (2014/02/14)

The calcium-dependent lipopeptide antibiotics represent a promising new class of antimicrobials for use in combating drug-resistant bacteria. At present, daptomycin is the only such lipopeptide used clinically and displays potent antimicrobial activity against a number of pathogenic Gram-positive bacteria. Given the increasing need for new antibiotics, practical synthetic access to unnatural analogues of daptomycin and related antimicrobial lipopeptides is of value. We here report an efficient synthetic route combining solid- and solution-phase techniques that allows for the rapid preparation of daptomycin analogues. Using this approach, four such analogues, including two enantiomeric variants, were synthesized and their antimicrobial activities and hydrolytic stabilities evaluated.

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