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411238-88-5

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411238-88-5 Usage

General Description

3-Hydrazinocarbonyl-pyrrolidine-1-carboxylic acid tert-butyl ester is a chemical compound with the molecular formula C11H20N4O3. It is a tert-butyl ester derivative of 3-hydrazinocarbonyl-pyrrolidine-1-carboxylic acid, a key intermediate in the synthesis of pharmaceuticals and biologically active compounds. 3-HYDRAZINOCARBONYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is a white crystalline solid that is soluble in organic solvents. It is commonly used as a building block in the synthesis of various drugs and bioactive molecules due to its versatile reactivity and functional group compatibility. Additionally, its tert-butyl ester form provides protection to the carboxylic acid functional group, allowing for controlled and selective manipulations in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 411238-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,1,2,3 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 411238-88:
(8*4)+(7*1)+(6*1)+(5*2)+(4*3)+(3*8)+(2*8)+(1*8)=115
115 % 10 = 5
So 411238-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H19N3O3/c1-10(2,3)16-9(15)13-5-4-7(6-13)8(14)12-11/h7H,4-6,11H2,1-3H3,(H,12,14)

411238-88-5 Well-known Company Product Price

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  • Aldrich

  • (ADE000050)  3-Hydrazinocarbonyl-pyrrolidine-1-carboxylic acid tert-butyl ester  AldrichCPR

  • 411238-88-5

  • ADE000050-1G

  • 1,930.50CNY

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411238-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-(hydrazinecarbonyl)pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Hydrazinocarbonyl-pyrrolidine-1-carboxylic acid tert-butyl ester

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:411238-88-5 SDS

411238-88-5Relevant articles and documents

1-CYANO-PYRROLIDINE DERIVATIVES AS DUB INHIBITORS

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Paragraph 0834-0835, (2020/11/30)

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of ubiquitin C-terminal hydrolase 30 or ubiquitin specific peptidase 30 (USP30). The novel compounds have formula (I): (Formula (I)) or are pharmaceutically acceptable salts thereof, wherein: R1a, R1b, R1c, R1d, R1e and R1f each independently represent hydrogen, optionally substituted C1-C6 alkyl or optionally substituted C3-C4 cycloalkyl, or R1b and R1c together form an optionally substituted C3-C6 cycloalkyl ring, or R1d and R1e together form an optionally substituted C3-C6 cycloalkyl ring; R2 represents hydrogen or optionally substituted C1-C6 alkyl; A represents an optionally further substituted 5 to 10 membered monocyclic or bicyclic heteroaryl, heterocyclyl or aryl ring; L represents a covalent bond or linker; B represents an optionally substituted 3 to 10 membered monocyclic or bicyclic heterocyclyl, heteroaryl, cycloalkyl or aryl ring; and when -A-L-B is at position x attachment to A is via a carbon ring atom of A, and either: A cannot be triazolopyridazinyl, triazolopyridinyl, imidazotriazinyl, imidazopyrazinyl or pyrrolopyrimidinyl; or B cannot be substituted with phenoxyl; or B cannot be cyclopentyl when L is an oxygen atom.

BIARYL CARBOXAMIDES

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Page/Page column 44-45, (2010/08/04)

This invention provides compounds of Formula (I) which are PAFR antagonists: Formula (I) and the pharmaceutically acceptable salts thereof. The compounds are useful for treating PAF-mediated disorders, and can be used in methods for treating atherosclerosis and preventing or reducing risk for atherosclerotic disease events. The compounds are also useful for treating or ameliorating pain, e.g. inflammatory pain and/or nociceptive pain, and for treating or ameliorating autoimmune and/or inflammatory diseases, among other conditions.

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