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17083-23-7

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  • 2-Methyl-2-propanyl O-(2-methyl-2-propanyl)-L-tyrosinate hydrochloride (1:1) Manufacturer/High quality/Best price/In stock

    Cas No: 17083-23-7

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17083-23-7 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 17083-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17083-23:
(7*1)+(6*7)+(5*0)+(4*8)+(3*3)+(2*2)+(1*3)=97
97 % 10 = 7
So 17083-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H27NO3/c1-16(2,3)20-13-9-7-12(8-10-13)11-14(18)15(19)21-17(4,5)6/h7-10,14H,11,18H2,1-6H3/t14-/m0/s1

17083-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (2S)-2-amino-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoate,hydrochloride

1.2 Other means of identification

Product number -
Other names L-tyrosine(tert-butyl ether)tert-butyl ester hydrochloride

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:17083-23-7 SDS

17083-23-7Relevant articles and documents

Conventional Synthesis of Thymopoietin 32-36 (TP 5) Using the 1-(1-Adamantyl)-1-methyletoxycarbonyl Group

Heinzel, Wolfgang,Kronbach, Thomas,Voelter, Wolfgang

, p. 1652 - 1658 (2007/10/02)

A synthesis of high yields of TP 5 is described.The α-amino functions were blocked by the acid-labile 1-(1-adamantyl)-1-methylethoxycarbonyl-(Adpoc)group.The Adpoc group is cleaved under mild acidolytic conditions with 3percent TFA in CH2Cl2 while the tert-butyl residues remained intact.This selective cleavage of the Adpoc group compared with the Boc and tert-butyl residues allows new strategies for the synthesis of large peptides. - Keywords: Adpoc, Amino acids, Thymopoietin

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