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909076-34-2

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909076-34-2 Usage

Description

1-tert-butyl 2-methyl 2-(3-chloropropyl)pyrrolidine-1,2-dicarboxylate is a complex chemical compound belonging to the pyrrolidine-1,2-dicarboxylate class. It features a pyrrolidine ring with a tert-butyl group, a methyl group, and a 3-chloropropyl group, along with two carboxylate functional groups. 1-tert-butyl 2-methyl 2-(3-chloropropyl)pyrrolidine-1,2-dicarboxylate is utilized in pharmaceutical research and drug development due to its potential pharmacological properties and may also find applications in organic synthesis and chemical reactions.

Uses

Used in Pharmaceutical Research and Drug Development:
1-tert-butyl 2-methyl 2-(3-chloropropyl)pyrrolidine-1,2-dicarboxylate is used as a research compound for exploring its pharmacological properties. Its unique molecular structure allows it to be studied for potential therapeutic applications in medicine.
Used in Organic Synthesis and Chemical Reactions:
In the field of organic synthesis, 1-tert-butyl 2-methyl 2-(3-chloropropyl)pyrrolidine-1,2-dicarboxylate serves as a versatile intermediate or reactant in various chemical reactions. Its functional groups and structural features enable it to participate in a range of synthetic processes, contributing to the development of new organic compounds and materials.
Proper handling and storage are essential for ensuring the safety and effectiveness of 1-tert-butyl 2-methyl 2-(3-chloropropyl)pyrrolidine-1,2-dicarboxylate in its intended applications.

Check Digit Verification of cas no

The CAS Registry Mumber 909076-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,0,7 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 909076-34:
(8*9)+(7*0)+(6*9)+(5*0)+(4*7)+(3*6)+(2*3)+(1*4)=182
182 % 10 = 2
So 909076-34-2 is a valid CAS Registry Number.

909076-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-tert-butyl 2-O-methyl 2-(3-chloropropyl)pyrrolidine-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1-tert-butyl 2-methyl 2-(3-chloropropyl)pyrrolidine-1,2-dicarboxylate

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:909076-34-2 SDS

909076-34-2Downstream Products

909076-34-2Relevant articles and documents

QUINAZOLINE COMPOUNDS, PREPARATION METHODS AND USES THEREOF

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Paragraph 183-184, (2022/01/12)

Provided herein are novel compounds, for example, compounds having a Formula (I), Formula (II), or Formula (III), or a pharmaceutically acceptable salt thereof. Also provided herein are methods of preparing the compounds and methods of using the compounds, for example, in inhibiting KRAS G12D in a cancer cell, and/or in treating various cancer such as pancreatic cancer, colorectal cancer, lung cancer or endometrial cancer.

A α - aza volute apperception preparation method of compound (by machine translation)

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Paragraph 0098; 0100; 0101; 0102, (2017/07/22)

The present invention provides a compound of α - aza volute apperception preparation method, with amino protective agent will be proline or 2 - piperidine carboxylic acid derivatives by reduction, oxidation, reductive amination, cyclization and other four-step reaction to obtain the α - aza spiro compound. The method of the invention only need 4 step reaction can be completed target preparation, simple and convenient operation, the four-step high overall yield, is usually 51.5% - 66.7%; to avoid the use of expensive and dangerous reagent, with the value of the large-scale preparation of the synthetic method. (by machine translation)

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