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849935-85-9

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849935-85-9 Usage

Description

(3S,4R)-1-tert-butyl 3-ethyl 4-hydroxypyrrolidine-1,3-dicarboxylate is a chiral organic compound characterized by its specific stereochemistry and functional groups. It features a pyrrolidine ring with a hydroxyl group and two carboxylate groups, as well as a tert-butyl and an ethyl substituent. (3S,4R)-1-tert-butyl 3-ethyl 4-hydroxypyrrolidine-1,3-dicarboxylate is known for its potential applications in the synthesis of biologically active molecules.

Uses

Used in Pharmaceutical Industry:
(3S,4R)-1-tert-butyl 3-ethyl 4-hydroxypyrrolidine-1,3-dicarboxylate is used as an intermediate in the preparation of various substituted fused quadracyclic compounds. These compounds are of interest due to their potential as inhibitors of MK2, a kinase enzyme involved in inflammatory and stress response pathways. By targeting MK2, these quadracyclic compounds may offer therapeutic benefits in treating conditions associated with excessive inflammation or cellular stress.
Additionally, the chiral nature and unique functional groups of (3S,4R)-1-tert-butyl 3-ethyl 4-hydroxypyrrolidine-1,3-dicarboxylate make it a valuable building block for the development of other pharmaceutical agents with specific biological activities. Its use in the synthesis of such compounds can lead to the discovery of new drugs with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 849935-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,9,3 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849935-85:
(8*8)+(7*4)+(6*9)+(5*9)+(4*3)+(3*5)+(2*8)+(1*5)=239
239 % 10 = 9
So 849935-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO5/c1-5-12(9(15)16)7-13(6-8(12)14)10(17)18-11(2,3)4/h8,14H,5-7H2,1-4H3,(H,15,16)/t8-,12-/m0/s1

849935-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-3-ethyl-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names S11-0055

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:849935-85-9 SDS

849935-85-9Downstream Products

849935-85-9Relevant articles and documents

TLR2 MODULATOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF

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Paragraph 00487-00488, (2021/12/08)

The present disclosure relates to compounds which modulate the activity of Toll-like receptor (TLR) proteins, including agonists or activators, partial agonists, and antagonists. Of particular interest of compounds that modulate the activity of TLR2, as well as methods of using such compounds to treat cancer and other disorders associated with a TLR2 pathway.

Synthesis, antimycobacterial and antibacterial activity of fluoroquinolone derivatives containing an 3-alkoxyimino-4-(cyclopropylanimo)methylpyrrolidine moiety

Zhang, Tingting,Shen, Weiyi,Liu, Mingliang,Zhang, Rui,Wang, Minghua,Li, Linhu,Wang, Bin,Guo, Huiyuan,Lu, Yu

, p. 73 - 85 (2015/10/19)

A series of novel fluoroquinolone derivatives containing an 3-alkoxyimino-4-(cyclopropylanimo)methylpyrrolidine moiety were designed, synthesized and evaluated for their biological activity. Our results revealed that 19b2 shows good activity against MTB H

Peptides containing an arginine mimetic for the treatment of bone metabolic disorders, their production, and drugs containing these compounds

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, (2008/06/13)

Arginine mimetic peptides according to Formula I of this application have a stimulating effect on bone formation and are useful for the treatment of bone metabolic disorders.

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