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113850-77-4

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113850-77-4 Usage

General Description

"(S)-Methyl2-amino-3-(4-iodophenyl)propanoate" is an organic compound that belongs to the class of chemical entities known as phenylpropanes. These are organic compounds containing a phenylpropane moiety. The "(S)" in its name refers to the chirality of the carbon atom, denoting it has a certain arrangement of its atoms in space. This chemical compound contains an iodine atom bound to a phenyl ring, a methyl ester group and an amino group. The details pertaining to its physical properties, uses, and toxicity are not abundantly available, indicating it might not be a widely used or studied compound. It's important to keep in mind any potential safety precautions or necessary handling guidelines due to the presence of iodine, which can be hazardous in certain forms and concentrations.

Check Digit Verification of cas no

The CAS Registry Mumber 113850-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,8,5 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113850-77:
(8*1)+(7*1)+(6*3)+(5*8)+(4*5)+(3*0)+(2*7)+(1*7)=114
114 % 10 = 4
So 113850-77-4 is a valid CAS Registry Number.

113850-77-4Downstream Products

113850-77-4Relevant articles and documents

Identification of inhibitors of UDP-galactopyranose mutaseviacombinatorialin situscreening

Fu, Jian,Fu, Huixiao,Xia, Yufen,N'Go, Inès,Cao, Jun,Pan, Weidong,Vincent, Stéphane P.

, p. 1818 - 1826 (2021)

Anin situscreening assay for UDP-galactopyranose mutase (UGM, an essential enzyme ofM. tuberculosiscell wall biosynthesis) has been developed to discover novel UGM inhibitors. The approach is based on the amide-forming reaction of an amino acid core with various cinnamic acids, followed by a direct fluorescence polarization assay to identify the best UGM binders without isolation and purification of the screened ligands. This assay allows us to perform one-pot high-throughput synthesis and screening of enzyme inhibitors in a 384-well plate format. UGM ligands were successfully identified by this technology and their inhibition levels were established from pure synthetic compoundsin vitroand in a whole cell antibacterial assay. This study provides a blueprint for designing enamide structures as new UGM inhibitors and anti-mycobacterial agents.

X???X Halogen Bond-Induced Supramolecular Helices

Hao, Aiyou,Xing, Pengyao,Xu, Yunying

supporting information, (2021/11/30)

The halogen bond is the attractive interaction between the electrophilic region of a halogen atom and the nucleophilic region of another molecular entity, emerging as a favorable manner to manipulate supramolecular chirality in self-assemblies. Engineerin

PENTAFLUOROPHOSPHATE DERIVATIVE, ITS USES AND AN APPROPRIATE MANUFACTURING METHOD

-

, (2019/04/05)

The invention relates to a pentafluorophosphate derivative according to general formula (I): or a pharmaceutically acceptable salt or solvate thereof. Thereby, R1 and R2 denote independently from each other H or F; R3 denotes H, an optionally substituted C1-C10 alkyl, an optionally substituted C3-C10 cycloalkyl, or an optionally substituted C6-C20 aryl, wherein a hydrocarbon chain of the alkyl, the cycloalkyl or the aryl can be interrupted by one or more oxygen, sulfur and/or nitrogen atoms; and M denotes any cation; with the proviso that at least one of R1 and R2 denotes F, if R3 denotes H. The invention further relates to uses of such a pentafluorophosphate derivative and to an appropriate manufacturing method.

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