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L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl-D-alanyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94849-38-4

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94849-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94849-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,4 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94849-38:
(7*9)+(6*4)+(5*8)+(4*4)+(3*9)+(2*3)+(1*8)=184
184 % 10 = 4
So 94849-38-4 is a valid CAS Registry Number.

94849-38-4SDS

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 Boc-L-Tyr-D-Ala-L-Phe-OH

1.2 Other means of identification

Product number -
Other names Boc-Tyr-D-Ala-Phe-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:94849-38-4 SDS

94849-38-4Downstream Products

94849-38-4Relevant academic research and scientific papers

Opioid Tripeptides Hybridized with trans-1-Cinnamylpiperazine as Proliferation Inhibitors of Pancreatic Cancer Cells in Two- and Three-Dimensional in vitro Models

Laskowska, Anna K.,Puszko, Anna K.,Sosnowski, Piotr,Ró?ycki, Krzysztof,Kosson, Piotr,Matalińska, Joanna,Durlik, Marek,Misicka, Aleksandra

, p. 1637 - 1644 (2017/10/07)

According to the World Health Organization, the mortality rate among patients with pancreatic cancer will increase in the upcoming years. Gemcitabine is the first choice for treatment of pancreatic malignancy, but increasing resistance to this drug is dec

Kinetically controlled peptide synthesis mediated by papain using the carbamoylmethyl ester as an acyl donor

Miyazawa, Toshifumi,Horimoto, Takao,Tanaka, Kayoko

, p. 371 - 376 (2014/08/18)

A series of dipeptides were synthesized generally in good yields with carbamoylmethyl (Cam) esters as acyl donors in the presence of a cysteine protease, papain, immobilized on Celite. Several segment condensations were also achieved generally in high yields without danger of racemization and formation of the secondary-hydrolysis product. Moreover, partial sequences of some bioactive peptides were prepared through segment condensations, and aimed-at peptides were obtained generally in high yields without the racemization of C-terminal residues of the carboxyl components. Thus, the superiority of the Cam ester in the kinetically controlled peptide synthesis was once again ascertained in couplings mediated by the cysteine protease as in those catalyzed by the serine proteases reported earlier.

Unique sequence in deltorphin C confers structural requirement for δ opioid receptor selectivity

Lazarus, LH,Salvadori, S,Grieco, P,Wilson, WE,Tomatis, R

, p. 791 - 797 (2007/10/02)

A series of deltorphin C (H-Tyr-D-Ala-Phe-Asp-Val-Val-Gly-NH2) analogues were synthesized to assess the consequences of changing anionic and hydrophobic residues on δ receptor selectivity.Analogues with altered C-terminal groups, inverted sequences, or es

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