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Carbamic acid, [(1S)-1-formyl-4-oxo-4-[(triphenylmethyl)amino]butyl]-, 9H-fluoren-9-ylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

334918-39-7

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  • 9H-Fluoren-9-ylmethyl N-[(2S)-1-oxo-4-[(triphenyl-methyl)carbamoyl]butan-2-yl]carbamate

    Cas No: 334918-39-7

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334918-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334918-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,9,1 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 334918-39:
(8*3)+(7*3)+(6*4)+(5*9)+(4*1)+(3*8)+(2*3)+(1*9)=157
157 % 10 = 7
So 334918-39-7 is a valid CAS Registry Number.

334918-39-7SDS

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 N-α-Fmoc-N-γ-trityl-glutaminal

1.2 Other means of identification

Product number -
Other names Fmoc-Gln(Trt)-H

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:334918-39-7 SDS

334918-39-7Relevant articles and documents

1,2,3-Triazoles as amide bond mimics: Triazole scan yields protease-resistant peptidomimetics for tumor targeting

Valverde, Ibai E.,Bauman, Andreas,Kluba, Christiane A.,Vomstein, Sandra,Walter, Martin A.,Mindt, Thomas L.

, p. 8957 - 8960 (2013/09/02)

The triazole makes the difference: Replacement of amide bonds in the backbone of peptides by 1,4-disubstituted 1,2,3-triazole isosteres affords peptidomimetics with retained receptor affinity and cell-internalization properties, enhanced proteolytic stability, and improved tumor-targeting capabilities. Copyright

Synthesis of a PNA-encoded cysteine protease inhibitor library

Debaene, Fran?ois,Mejias, Lorenzo,Harris, Jennifer L.,Winssinger, Nicolas

, p. 8677 - 8690 (2007/10/03)

Peptide nucleic acids (PNAs) have been used to encode a combinatorial library whereby each compound is labeled with a PNA tag which reflects its synthetic history and localizes the compound upon hybridization to an oligonucleotide array. We report herein

Combinatorial Synthesis of a Small-Molecule Library Based on the Vinyl Sulfone Scaffold

Wang, Gang,Yao, Shao Q.

, p. 4437 - 4440 (2007/10/03)

(Equation presented) A 30-member library of small molecules based on the vinyl sulfone scaffold was prepared on rink amide resin, using solid phase-based reactions such as oxidation and Horner-Wadsworth-Emmons reaction. The library was designed such that

Solid-phase synthesis of peptide vinyl sulfones as potential inhibitors and activity-based probes of cysteine proteases

Wang, Gang,Mahesh, Uttamchandani,Chen, Grace Y. J.,Yao, Shao Q.

, p. 737 - 740 (2007/10/03)

(Matrix presented) Peptide vinyl sulfones were prepared from 2-chlorotrityl resin-bound phenolic amino vinyl sulfones in high yield and purity. This method enables the convenient synthesis of peptide vinyl sulfones having different amino acids at the Psu

Sequencing hydroxyethylamine-containing peptides via Edman degradation

Brewer, Matthias,Oost, Thorsten,Sukonpan, Chanokporn,Pereckas, Michael,Rich, Daniel H.

, p. 3469 - 3472 (2007/10/03)

(matrix presented) Hydroxyethylamine-containing peptides can be sequenced by automated Edman degradation to provide sequence information for peptide segments on either side of the peptide backbone modification.

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