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82038-34-4

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  • (2s)-3-(4-hydroxyphenyl)-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic Acid CAS NO.82038-34-4

    Cas No: 82038-34-4

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82038-34-4 Usage

Chemical Properties

Colourless Oil

Uses

BOC-N-ME-TYR-OH is used in the preparation of tyrosyl derivatives as P2X7 receptor modulators.

Check Digit Verification of cas no

The CAS Registry Mumber 82038-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,3 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82038-34:
(7*8)+(6*2)+(5*0)+(4*3)+(3*8)+(2*3)+(1*4)=114
114 % 10 = 4
So 82038-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO5.C12H23N/c1-15(2,3)21-14(20)16(4)12(13(18)19)9-10-5-7-11(17)8-6-10;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h5-8,12,17H,9H2,1-4H3,(H,18,19);11-13H,1-10H2/t12-;/m0./s1

82038-34-4SDS

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 (2S)-3-(4-hydroxyphenyl)-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid

1.2 Other means of identification

Product number -
Other names Boc-N-Me-Tyr-OH.DCHA

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:82038-34-4 SDS

82038-34-4Relevant articles and documents

Conjugate of cytotoxin molecule and cell binding receptor molecule

-

Paragraph 0051; 0420-0422, (2019/10/10)

A conjugate of a strong cytotoxin molecule and a cell binding receptor molecule has a structure shown in a molecular formula (I), wherein T, L, m, n, -----, R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12 and R13 are defined in the text. The conjugate is used for treating cancer, immunological diseases and infectious diseases.

Synthesis of (9R,12S)- and (9S,12S)-cycloisodityrosine and their N-methyl derivatives

Boger, Dale L.,Zhou, Jiacheng,Borzilleri, Robert M.,Nukui, Seiji,Castle, Steven L.

, p. 2054 - 2069 (2007/10/03)

Full details of the synthesis of (9R,12S)- and (9S,12S)-cycloisodityrosine and their N-methyl derivatives are detailed based on an intramolecular nucleophilic aromatic substitution reaction for formation of the key biaryl ether with 14-membered ring macrocyclization. Their comparison with prior samples and the documentation of a facile C9 epimerization within the natural 9S series are described.

Studies on the total synthesis of bouvardin and deoxybouvardin: Cyclic hexapeptide cyclization studies and preparation of key partial structures

Boger,Yohannes

, p. 487 - 499 (2007/10/02)

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