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117175-41-4

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117175-41-4 Usage

General Description

"(R)-2-thiocarbamoyl-pyrrolidine-1-carboxylic acid tert-butyl ester" is a chemical compound with the molecular formula C10H19NO2S. It is a tert-butyl ester derivative of (R)-2-thiocarbamoyl-pyrrolidine-1-carboxylic acid, and is commonly used in organic synthesis and pharmaceutical research. (R)-2-THIOCARBAMOYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER has been studied for its potential medical applications, and its properties make it suitable for use as an intermediate in the synthesis of various biologically active molecules. It is important to handle this chemical with care, as it may have potential health and environmental hazards if not used properly and disposed of responsibly.

Check Digit Verification of cas no

The CAS Registry Mumber 117175-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,7 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 117175-41:
(8*1)+(7*1)+(6*7)+(5*1)+(4*7)+(3*5)+(2*4)+(1*1)=114
114 % 10 = 4
So 117175-41-4 is a valid CAS Registry Number.

117175-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-THIOCARBAMOYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

1.2 Other means of identification

Product number -
Other names Boc-L-Pyroglutaminol

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:117175-41-4 SDS

117175-41-4Relevant articles and documents

Synthetic Studies on Alotamide A: Construction of N-Demethylalotamide A

Domínguez, Marta,Román, David,Souto, José A.,de Lera, ángel R.

, p. 6057 - 6070 (2021/12/10)

Several approaches to the synthesis of cyclodepsipeptide natural product alotamide A are described, eventually affording a very advanced N-demethylated analogue of the targeted natural product. The difficulties found in our endeavors on the synthesis of alotamide A have allowed us to gather some valuable information regarding the most convenient synthetic step for each key transformation. The intramolecular Csp2?Csp2 Stille cross-coupling and the macrolactam formation were found to be reliable protocols for the final construction of the alotamide A skeleton.

MDM2 DEGRADERS AND USES THEREOF

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Paragraph 001326; 001327-001328, (2021/09/26)

The present invention relates to compounds and methods useful for the modulation of mouse double minute 2 homolog ("MDM2") protein via ubiquitination and/or degradation by compounds according to the present invention.

IRAK DEGRADERS AND USES THEREOF

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Paragraph 00962; 001086-001088, (2020/06/19)

The present invention provides compounds, compositions thereof, and methods of using the same.

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