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Carbamic acid, [2-azido-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, 1,1-dimethylethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71591-33-8

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71591-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71591-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,9 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71591-33:
(7*7)+(6*1)+(5*5)+(4*9)+(3*1)+(2*3)+(1*3)=128
128 % 10 = 8
So 71591-33-8 is a valid CAS Registry Number.

71591-33-8SDS

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 Boc-Tyr-azide

1.2 Other means of identification

Product number -
Other names Boc-Tyr-N3

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:71591-33-8 SDS

71591-33-8Relevant academic research and scientific papers

Efficient synthesis of O-succinimidyl-(tert-butoxycarbonylamino)methyl carbamates derived from α-amino acids accelerated by ultrasound: Application to the synthesis of ureidodipeptides

Sureshbabu, Vommina V.,Sudarshan, Naremaddepalli S.,Kantharaju

, p. 2168 - 2184 (2008/09/21)

The synthesis of O-succinimidyl-(tert-butoxycarbonylamino)methyl carbamates employing isocyanates made through the Curtius rearrangement of Boc-amino acid azides in the presence of N-hydroxysuccinimide under the influence of ultrasound is described. Copyright Taylor & Francis Group, LLC.

Oral Bioavailability of a New Class of μ-Opioid Receptor Agonists Containing 3,6-Bis[Dmt-NH(CH2)n]-2(1H)-pyrazinone with Central-Mediated Analgesia

Jinsmaa, Yunden,Miyazaki, Anna,Fujita, Yoshio,Li, Tingyou,Fujisawa, Yutaka,Shiotani, Kimitaka,Tsuda, Yuko,Yokoi, Toshio,Ambo, Akihiro,Sasaki, Yusuke,Bryant, Sharon D.,Lazarus, Lawrence H.,Okada, Yoshio

, p. 2599 - 2610 (2007/10/03)

The inability of opioid peptides to be transported through epithelial membranes in the gastrointestinal tract and pass the blood-brain barrier limits their effectiveness for oral application in an antinociceptive treatment regime. To overcome this limitat

Chemical Synthesis of Fully Active and Heat-stable Fragments of Heat-stable Enterotoxin of Enterotoxigenic Escherichia coli Strain 18D

Yoshimura, Shoko,Takao, Toshifumi,Ikemura, Haruo,Aimoto, Saburo,Shimonishi, Yasutsugu,et al.

, p. 1381 - 1387 (2007/10/02)

Two shorter peptides of a heat-stable enterotoxin (STp), which is produced by enterotoxigenic Escherichia coli strain 18D, were prepared by two different procedures; i) chemical synthesis and ii) Edman-degradation of STp.These peptid

Synthesis and pharmacological activity of dermorphin tetrapeptide-analogs

Salvadori,Sarto,Tomatis

, p. 489 - 493 (2007/10/02)

The authors report on the synthesis and pharmacological activity of twenty-four tetrapeptide-analogs of the opioid heptapeptide dermorphin; their terminal amino group were replaced by guanidino functions and/or the C-termini were changed into amide moieti

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