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866114-96-7

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866114-96-7 Usage

Description

(S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid is a complex organic compound that belongs to the class of chemical compounds known as boronic acids. It is characterized by the presence of a boron atom bonded to an oxygen atom and two carbon atoms. The "S-" in its name signifies the stereochemistry, which refers to the spatial arrangement of atoms. (S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid features a benzyloxy group (a benzyl group bound to an oxygen atom) and a carboxyl group (COOH) with an additional benzyl group, suggesting potential applications in organic synthesis due to its ability to participate in various chemical reactions.

Uses

Used in Organic Synthesis:
(S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure, including the benzyloxy and carboxyl groups, allows it to undergo a range of chemical reactions, making it a valuable building block in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid is used as a key component in the development of new drugs. Its versatility in undergoing chemical reactions enables the creation of novel drug candidates with potential therapeutic applications.
Used in Material Science:
(S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid is used as a precursor in the synthesis of advanced materials, such as polymers and composites, with specific properties tailored for various applications. Its reactivity and functional groups contribute to the development of materials with improved performance characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 866114-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,1,1 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 866114-96:
(8*8)+(7*6)+(6*6)+(5*1)+(4*1)+(3*4)+(2*9)+(1*6)=187
187 % 10 = 7
So 866114-96-7 is a valid CAS Registry Number.

866114-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[(2S)-3-oxo-3-phenylmethoxy-2-(phenylmethoxycarbonylamino)propyl]phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names benzyl (S)-2-[(benzyloxycarbonyl)amino]-3-[4-(borono)phenyl]propionate

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:866114-96-7 SDS

866114-96-7Relevant articles and documents

Synthesis of the side chain cross-linked tyrosine oligomers dityrosine, trityrosine, and pulcherosine

Skaff, Ojia,Jolliffe, Katrina A.,Hutton, Craig A.

, p. 7353 - 7363 (2007/10/03)

An efficient synthesis of dityrosine and the first syntheses of the tyrosine trimers trityrosine and pulcherosine have been achieved. Protected 3-iodotyrosine underwent tandem Miyaura borylation-Suzuki coupling to give protected dityrosine. The choice of

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