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AC-PHE-TYR-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2365-53-9

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2365-53-9 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 2365-53-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2365-53:
(6*2)+(5*3)+(4*6)+(3*5)+(2*5)+(1*3)=79
79 % 10 = 9
So 2365-53-9 is a valid CAS Registry Number.

2365-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name AC-PHE-TYR-OH

1.2 Other means of identification

Product number -
Other names N-ACETYL-L-PHE-3,5-DIIODO-L-TYR

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:2365-53-9 SDS

2365-53-9Downstream Products

2365-53-9Relevant academic research and scientific papers

Improved method for the synthesis of pentaphenylcyclopentadiene

Dyumaev, V. K.,Davydov, D. V.,Beletskaya, I. P.

, p. 571 - 573 (1993)

An improved method for the synthesis of pentaphenylcyclopentadiene is suggested.It involves the reaction of tetraphenylcyclopentadienone with PhMgBr and subsequent treatment of the reaction mixture with an excess of LiAlH4 in THF.The effect of arylating agents and reducing agents on the yield of the target product is studied.The method suggested can be used for synthesizing other polyaromatic cyclopentadienes, in particular, 1,2,5-triphenyl-3,4-(1,8-naphthylene)cyclopentadiene.

Asymmetric hydrogenation of N-acetylhydrodipeptide complexes with Mg(II) and C(II) ions

Lisichkina, I. N.,Vinogradova, A. I.,Sukhorukova, N. B.,Tselyapina, E. V.,Saporovskaya, M. B.,Belikov, V. M.

, p. 569 - 571 (2007/10/02)

N-Ac-Δ-Phe-AA form labile complexes with Mg(II) ions.Potentiometric titration data show that the carboxyl group of the dehydropeptide in them scarcely participates in complexation, unlike the complexes with Ca(II) ions.The hydrogenation of these complexes

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