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514214-66-5

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514214-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 514214-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,4,2,1 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 514214-66:
(8*5)+(7*1)+(6*4)+(5*2)+(4*1)+(3*4)+(2*6)+(1*6)=115
115 % 10 = 5
So 514214-66-5 is a valid CAS Registry Number.

514214-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Boc-L-Phe-Bt

1.2 Other means of identification

Product number -
Other names Boc-Phe-Bt

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:514214-66-5 SDS

514214-66-5Relevant articles and documents

Total Synthesis of Pyrophen and Campyrones A-C

Reber, Keith P.,Burdge, Hannah E.

, p. 292 - 297 (2018)

The first total syntheses of the natural products pyrophen and campyrones A-C, isolated from the fungus Aspergillus Niger, have been achieved in six steps starting from commercially available N-Boc amino acids. Key steps in this sequence include a vinylog

Design, synthesis, antimicrobial, and DNA gyrase inhibitory properties of fluoroquinolone–dichloroacetic acid hybrids

Seliem, Israa A.,Panda, Siva S.,Girgis, Adel S.,Nagy, Yosra I.,George, Riham F.,Fayad, Walid,Fawzy, Nehmedo G.,Ibrahim, Tarek S.,Al-Mahmoudy, Amany M. M.,Sakhuja, Rajeev,Abdel-samii, Zakaria K. M.

, p. 248 - 259 (2019/11/14)

A series of new fluoroquinolone conjugates 8a–g and 9a–f were synthesized via benzotriazole-mediated synthetic approach with good yield and purity. Some of the synthesized analogs exhibited significant antibacterial properties against Escherichia coli and

A simple and versatile method to synthesize N-acyl-benzotriazoles

Laconde, Guillaume,Amblard, Muriel,Martinez, Jean

supporting information, p. 341 - 343 (2019/01/04)

An efficient method for the synthesis of N-acyl-benzotriazoles from a wide variety of protected amino acids, as well as from compounds frequently used in drug discovery such as biotin and N-Fmoc polyethylene glycol, has been developed. The reaction of car

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