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(S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is a complex organic compound characterized by a propanoic acid core, with a tert-butoxycarbonylamino group and a pent-4-enyloxy side chain. The presence of a chiral center in its structure indicates the existence of stereoisomers, with the (S)-enantiomer being specifically denoted. (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is likely to have applications in medicinal and pharmaceutical chemistry due to the known anti-inflammatory and analgesic properties of propanoic acids, and the boc-protected amino group suggests its potential use in peptide synthesis or drug delivery systems.

790305-00-9

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790305-00-9 Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is used as a pharmaceutical intermediate for the development of new drugs, leveraging its anti-inflammatory and analgesic properties inherent to propanoic acids.
Used in Peptide Synthesis:
In the field of organic chemistry, (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid serves as a building block in peptide synthesis, where the boc-protected amino group is crucial for the stepwise assembly of peptide chains.
Used in Drug Delivery Systems:
(S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is utilized in the design of drug delivery systems to improve the bioavailability and targeting of therapeutic agents, taking advantage of its structural features to enhance drug efficacy and reduce side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 790305-00-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,3,0 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 790305-00:
(8*7)+(7*9)+(6*0)+(5*3)+(4*0)+(3*5)+(2*0)+(1*0)=149
149 % 10 = 9
So 790305-00-9 is a valid CAS Registry Number.

790305-00-9SDS

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 (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pent-4-enoxypropanoic acid

1.2 Other means of identification

Product number -
Other names -

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:790305-00-9 SDS

790305-00-9Relevant articles and documents

Water-soluble poly(l -serine)s with elongated and charged side-chains: Synthesis, conformations, and cell-penetrating properties

Tang, Haoyu,Yin, Lichen,Lu, Hua,Cheng, Jianjun

, p. 2609 - 2615 (2012)

Water-soluble poly(l-serine)s bearing long side-chain with terminal charge groups were synthesized via ring-opening polymerization of O-pentenyl-l-serine N-carboxyanhydride followed by thiol-ene reactions. These side-chain modified poly(l-serine)s adopt β

Genetically encoded alkenes in yeast

Ai, Hui-Wang,Shen, Weijun,Brustad, Eric,Schultz, Peter G.

, p. 935 - 937 (2010)

(Figure Presented) Olefin-containing amino acids have been genetically introduced into proteins in Saccharomyces cerevisiae by orthogonal tRNA/aminoacyl-tRNA synthetase pairs. These nonnatural amino acids can be used for selective protein modification thr

Stable helical ionic polypeptides

-

Page/Page column 119-121, (2016/02/12)

The invention provides polymers comprising Formula I: wherein monomer is a repeating unit comprising 2, 3, 4, 5, 6 or 7 carbon atoms and the monomers are linked together through amide or ester bonds; n is about 6 to about 1000; and Linker is an optionally

A concise synthesis of the HCV protease inhibitor BILN 2061 and its P3 modified analogs

Liu, Dejun,Dong, Jingchao,Yin, Yunxing,Ma, Rujian,Shi, Yifeng,Wu, Hao,Chen, Shuhui,Li, Ge

experimental part, p. 1489 - 1502 (2011/11/01)

A concise synthesis of BILN 2061 was achieved through more efficient installation of P2 4-quinoline moiety via SN2 displacement of the β-OBs group located on the 4-hydroxyl proline intermediate, which was prepared from 4-α-hydroxyl proline analog via Mitsunobu reaction with inversion of stereochemistry. In addition, a short and practical synthesis for P3 unit is also described herein. Final assembly of four fragments for BILN 2061 was achieved with an overall yield of 58% in 4 steps from P1 to 15a. Furthermore several analogs of BILN 2061 (WX-1-WX-5) containing modifications on P3 unit were synthesized successfully using the same synthetic route as described for the parent inhibitor BILN 2061. Copyright

Inhibitors of Hepatitis C Virus

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Page/Page column 41, (2008/12/04)

Macrocyclic peptides are disclosed having the general formula: wherein R3, R3′, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

MACROCYCLIC PEPTIDES AS HEPATITIS C VIRUS INHIBITORS

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Page/Page column 84, (2008/12/05)

Macrocyclic peptides having the general formula (I): are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Inhibitors of Hepatitis C Virus

-

Page/Page column 39, (2008/12/04)

Macrocyclic peptides are disclosed having the general formula: wherein R3, R3′, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Inhibitors of Hepatitis C Virus

-

Page/Page column 40, (2008/12/04)

Macrocyclic peptides are disclosed having the general formula: wherein R3, R′3, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

MACROCYCLIC PEPTIDES AS HEPATITIS C VIRUS INHIBITORS

-

Page/Page column 81, (2008/12/05)

Macrocyclic peptides having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Hepatitis C virus inhibitors

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Page/Page column 54-55, (2010/11/26)

Hepatitis C virus inhibitors having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

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