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911050-87-8

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  • (S)-Methyl 4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoate

    Cas No: 911050-87-8

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  • (S)-Methyl 4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoate

    Cas No: 911050-87-8

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911050-87-8 Usage

Description

(S)-Methyl 4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoate is a complex chiral ester derivative utilized in organic chemistry. It features a benzyloxycarbonylamino group and a tert-butyldimethylsilyloxy group, making it a valuable building block for synthesizing complex molecules, including pharmaceuticals and natural products. Its chiral nature is crucial for creating enantiopure compounds, which are significant in drug development and organic chemistry. The tert-butyldimethylsilyloxy group acts as a protective group, enabling selective reactions with other functional groups.

Uses

Used in Pharmaceutical Industry:
(S)-Methyl 4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoate is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its chiral nature allows for the creation of enantiopure compounds, which are essential in drug development due to their potential for improved efficacy and reduced side effects.
Used in Natural Product Synthesis:
In the field of natural product synthesis, (S)-Methyl 4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoate is used as a building block for constructing complex natural products. Its structural features facilitate the development of novel compounds with potential biological activities.
Used in Organic Chemistry Research:
(S)-Methyl 4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoate serves as an important intermediate in organic chemistry research, particularly in the development of new synthetic methods and the exploration of novel reaction mechanisms. Its versatility and the presence of protective groups make it a valuable tool for chemists working on complex molecular structures.

Check Digit Verification of cas no

The CAS Registry Mumber 911050-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,0,5 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 911050-87:
(8*9)+(7*1)+(6*1)+(5*0)+(4*5)+(3*0)+(2*8)+(1*7)=128
128 % 10 = 8
So 911050-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H33NO5Si/c1-20(2,3)27(5,6)26-15-17(12-13-18(22)24-4)21-19(23)25-14-16-10-8-7-9-11-16/h7-11,17H,12-15H2,1-6H3,(H,21,23)

911050-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-[tert-butyl(dimethyl)silyl]oxy-4-(phenylmethoxycarbonylamino)pentanoate

1.2 Other means of identification

Product number -
Other names methyl (4S)-4-[(benzyloxy)carbonyl]amino-5-{[tert-butyldimethylsilyl]oxy}pentanoate

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:911050-87-8 SDS

911050-87-8Relevant articles and documents

Design and synthesis of an orally active matrix metalloproteinase inhibitor

Yamamoto, Shingo,Nakatani, Shingo,Ikura, Masahiro,Sugiura, Tsuneyuki,Nishita, Yoshitaka,Itadani, Satoshi,Ogawa, Koji,Ohno, Hiroyuki,Takahashi, Kanji,Nakai, Hisao,Toda, Masaaki

, p. 6383 - 6403 (2007/10/03)

A series of 4-(4-phenoxy)benzoylamino-4-methoxymethyloxymethyl butyric acid hydroxamates, which were derived from l-glutamic acid, were synthesized and evaluated as matrix metalloproteinase inhibitors. Most of the compounds listed in Tables 1-3 exhibited

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