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[2-(4-BROMO-PHENYL)-2-HYDROXY-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER is a chemical compound with the molecular formula C12H17BrNO3. It is a tert-butyl ester derivative of carbamic acid, featuring a bromo-phenyl group and a hydroxy-ethyl group. [2-(4-BROMO-PHENYL)-2-HYDROXY-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER is primarily utilized in the pharmaceutical industry as an intermediate for synthesizing a range of organic compounds, with potential applications in drug production and other pharmaceutical products.
Used in Pharmaceutical Industry:
[2-(4-BROMO-PHENYL)-2-HYDROXY-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure, which includes a bromo-phenyl group and a hydroxy-ethyl group, makes it a valuable component in the development of pharmaceutical products. The specific applications and properties of [2-(4-BROMO-PHENYL)-2-HYDROXY-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER can vary depending on the context in which it is being used, highlighting its versatility in the creation of new drugs and other pharmaceutical formulations.

913181-90-5

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913181-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913181-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,1,8 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 913181-90:
(8*9)+(7*1)+(6*3)+(5*1)+(4*8)+(3*1)+(2*9)+(1*0)=155
155 % 10 = 5
So 913181-90-5 is a valid CAS Registry Number.
InChI:InChI=1S/C13H18BrNO3/c1-13(2,3)18-12(17)15-8-11(16)9-4-6-10(14)7-5-9/h4-7,11,16H,8H2,1-3H3,(H,15,17)

913181-90-5SDS

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 tert-butyl N-[2-(4-bromophenyl)-2-hydroxyethyl]carbamate

1.2 Other means of identification

Product number -
Other names QC-7805

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:913181-90-5 SDS

913181-90-5Relevant academic research and scientific papers

Self-assembly of oxidation-responsive polyethylene glycol-paclitaxel prodrug for cancer chemotherapy

Dong, Chengyuan,Liu, Fusheng,Shen, Youqing,Xiang, Jiajia,Zhou, Quan,Zhou, Zhuxian

, p. 529 - 539 (2020/03/04)

Amphiphilic drug conjugates can self-assemble into nanovehicles for cancer drug delivery, but the key is to design stable yet intracellular labile drug linkers for drug retention during blood circulation but fast intracellular drug release. The conjugatio

Direct catalytic synthesis of unprotected 2-amino-1-phenylethanols from alkenes by using iron(II) phthalocyanine

Legnani, Luca,Morandi, Bill

supporting information, p. 2248 - 2251 (2016/02/18)

Aryl-substituted amino alcohols are privileged scaffolds in medicinal chemistry and natural products. Herein, we report that an exceptionally simple and inexpensive FeII complex efficiently catalyzes the direct transformation of simple alkenes into unprotected amino alcohols in good yield and perfect regioselectivity. This new catalytic method was applied in the expedient synthesis of bioactive molecules and could be extended to aminoetherification.

Synthesis and in vitro biological evaluation of aryl boronic acids as potential inhibitors of factor XIa

Lazarova, Tsvetelina I.,Jin, Lei,Rynkiewicz, Michael,Gorga, Joan C.,Bibbins, Frank,Meyers, Harold V.,Babine, Robert,Strickler, James

, p. 5022 - 5027 (2007/10/03)

A series of functionalized aryl boronic acids were synthesized and evaluated as potential inhibitors of factor XIa. Crystal structures of the protein-inhibitor complexes led to the design and synthesis of second generation compounds showing single digit m

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