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195325-55-4

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  • Large Stock 99.0% Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1 H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)- 195325-55-4 Producer

    Cas No: 195325-55-4

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  • Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1 H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)-

    Cas No: 195325-55-4

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  • Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1 H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)-

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  • Kono Chem Co.,Ltd
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  • Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1 H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)-

    Cas No: 195325-55-4

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195325-55-4 Usage

Description

Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)is a complex organic compound that features a carbamic acid core, a 1,1-dimethylethyl ester group, a methoxymethylamino moiety, and a sulfonyl-substituted indole group. This (S)-enantiomer possesses a distinct molecular structure, which endows it with unique properties and potential applications across various industries.

Uses

Used in Pharmaceutical Industry:
Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)is utilized as an active pharmaceutical ingredient for the development of new drugs. Its unique molecular structure allows it to interact with specific biological targets, potentially leading to the treatment of various diseases and medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)serves as a key component in the formulation of pesticides and herbicides. Its ability to target specific pests and weeds makes it a valuable tool in modern agriculture for increasing crop yields and protecting plants from damage.
Used in Materials Science:
Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-indol-3-yl]methyl]ethyl]-, 1,1-dimethylethyl ester, (S)is employed in the development of advanced materials with specialized properties. Its unique molecular structure can be leveraged to create materials with enhanced performance characteristics, such as improved strength, flexibility, or chemical resistance, for use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 195325-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,3,2 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 195325-55:
(8*1)+(7*9)+(6*5)+(5*3)+(4*2)+(3*5)+(2*5)+(1*5)=154
154 % 10 = 4
So 195325-55-4 is a valid CAS Registry Number.

195325-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name {(S)-1-(Methoxy-methyl-carbamoyl)-2-[1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indol-3-yl]-ethyl}-carbamic acid tert-butyl ester

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:195325-55-4 SDS

195325-55-4Downstream Products

195325-55-4Relevant articles and documents

A highly stereoselective synthesis of the functionalized (E)-alkene dipeptide isostere of Trp-Val via organocyanocopper-Lewis acid mediated reaction

Noda, Masaki,Ibuka, Toshiro,Habashita, Hiromu,Fujii, Nobutaka

, p. 1259 - 1264 (2007/10/03)

A stereocontrolled synthesis of the (e)-alkene dipeptide isostere of Trp-Val is described. The stereospecific α-alkylation of the δ-amino-γ- mesyloxy-α,β-unsaturated ester via the organocyanocopper-Lewis acid mediated reaction, based on 1,3-transfer of ch

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