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3392-15-2

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3392-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3392-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3392-15:
(6*3)+(5*3)+(4*9)+(3*2)+(2*1)+(1*5)=82
82 % 10 = 2
So 3392-15-2 is a valid CAS Registry Number.

3392-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-L-Phe-L-Tyr-OEt

1.2 Other means of identification

Product number -
Other names N-(N-Benzyloxycarbonyl-L-phenylalanyl)-L-tyrosin-aethylester

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:3392-15-2 SDS

3392-15-2Relevant articles and documents

Practical Peptide Synthesis Mediated by a Recyclable Hypervalent Iodine Reagent and Tris(4-methoxyphenyl)phosphine

Zhang, Chi,Liu, Shan-Shan,Sun, Bo,Tian, Jun

supporting information, p. 4106 - 4109 (2015/09/01)

6-(3,5-Bis(trifluoromethyl)phenyl)-1H,4H-2aλ3-ioda-2,3-dioxacyclopenta[hi]indene-1,4-dione (p-BTFP-iodosodilactone, 1a) was synthesized and demonstrated to be an efficient hypervalent iodine(III) reagent for the synthesis of dipeptides from various standard amino acids, including sterically hindered amino acids, in good to high yields within 30 min in the presence of tris(4-methoxyphenyl)phosphine. In addition, the combined system of 1a/(4-MeOC6H4)3P was used to synthesize the pentapeptide leu-enkephalin in protected form. It is worth noting that 1a can be regenerated readily after reaction.

Discovery of potent and selective phenylalanine derived CCR3 antagonists. Part 1

Dhanak, Dashyant,Christmann, Lisa T.,Darcy, Michael G.,Jurewicz, Anthony J.,Keenan, Richard M.,Lee, Judithann,Sarau, Henry M.,Widdowson, Katherine L.,White, John R.

, p. 1441 - 1444 (2007/10/03)

The discovery of a series of phenylalanine derived CCR3 antagonists is reported. Parallel, solution-phase library synthesis has been utilized to delineate the structure-activity relationship leading to the synthesis of highly potent, CCR3-selective antagonists.

A novel support for enzyme adsorption: Properties and applications of aerogels in low water media

Basso,De Martin,Ebert,Gardossi,Tomat,Casarci,Li Rosi

, p. 8627 - 8630 (2007/10/03)

Aerogels, because of their porosity, have a great ability to adsorb water, and this characteristic was exploited to extend the applicability of aerogels for the adsorption and entrapment of hydrolases to be used in organic media. The applicability of aero

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