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Ethyl 2-bromothiazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41731-83-3

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41731-83-3 Usage

Uses

Ethyl 2-bromothiazole-5-carboxylate is used in medicine, pharmaceutical intermediate

Check Digit Verification of cas no

The CAS Registry Mumber 41731-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41731-83:
(7*4)+(6*1)+(5*7)+(4*3)+(3*1)+(2*8)+(1*3)=103
103 % 10 = 3
So 41731-83-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrNO2S/c1-2-10-5(9)4-3-8-6(7)11-4/h3H,2H2,1H3

41731-83-3 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H55109)  Ethyl 2-bromothiazole-5-carboxylate, 98%   

  • 41731-83-3

  • 250mg

  • 235.0CNY

  • Detail
  • Alfa Aesar

  • (H55109)  Ethyl 2-bromothiazole-5-carboxylate, 98%   

  • 41731-83-3

  • 1g

  • 657.0CNY

  • Detail
  • Alfa Aesar

  • (H55109)  Ethyl 2-bromothiazole-5-carboxylate, 98%   

  • 41731-83-3

  • 5g

  • 2769.0CNY

  • Detail
  • Aldrich

  • (642495)  Ethyl2-bromothiazole-5-carboxylate  97%

  • 41731-83-3

  • 642495-1G

  • 1,045.98CNY

  • Detail
  • Aldrich

  • (642495)  Ethyl2-bromothiazole-5-carboxylate  97%

  • 41731-83-3

  • 642495-5G

  • 4,409.73CNY

  • Detail

41731-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-bromothiazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Bromo-5-(ethoxycarbonyl)thiazole

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:41731-83-3 SDS

41731-83-3Relevant academic research and scientific papers

Five-membered heteroaromatic derivative, preparation method and application thereof

-

Paragraph 0583-0587, (2021/07/08)

The invention belongs to the technical field of medicines, and particularly relates to a five-membered heteroaromatic compound, a composition, a preparation method and application thereof. The compound or the composition can be used as an inhibitor of a retinoid-related orphan receptor [gamma]t (ROR [gamma]t). The invention also relates to a method for preparing the compound and the composition, and application of the compound and the composition in treatment or prevention of ROR [gamma]t-mediated cancers, inflammations or autoimmune diseases of mammals, especially human beings.

COMPOUNDS AND COMPOSITIONS FOR USE IN TREATING SKIN DISORDERS

-

Paragraph 1426-1428, (2021/08/06)

Provided herein is a compound of formula (XXXII) or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer thereof or a physiologically functional derivative thereof, wherein R1, R2, R3, G, A, E, n, p, and q are defined herein. Also provided herein are compositions comprising a compound of formula (XXXII), and methods of using a compound of formula (XXXII), e.g., in the treatment or prevention of skin disorders.

ACID ADDITION SALTS OF PIPERAZINE DERIVATIVES

-

Page/Page column 52; 53, (2017/09/09)

The invention relates to acid addition salts of piperazine derivatives, as well as solid forms, such as polymorphic forms, thereof, which are useful as pharmaceutical ingredients and in particular as glycosidase inhibitors.

PROCESS FOR THE SEPARATION OF ENANTIOMERS OF PIPERAZINE DERIVATIVES

-

Page/Page column 46; 47, (2017/09/21)

The invention relates to a process for preparing either enantiomer of a compound of formula (I), wherein X, Y and n have the meaning given in claim 1, with high enantiomeric excess (e.e.), by chiral resolution in the presence of a non-racemic, chiral acid.

GLYCOSIDASE INHIBITORS

-

Page/Page column 118-119, (2016/03/22)

Compounds of formula (I) wherein A, R, W, Q, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

GLYCOSIDASE INHIBITORS

-

Page/Page column 87; 88, (2014/10/15)

Compounds of formula (I) wherein X1, X2, W, R1 to R5, L and m have the meaning according to the claims, are glucosidase inhibitors, and can be employed, inter alia, for the treatment of Alzheimer's disease.

Regioselective functionalization of the thiazole scaffold using TMPMgCl?LiCl and TMP2Zn?2MgCl2?2LiCl

Dunst, Cora,Knochel, Paul

experimental part, p. 6972 - 6978 (2011/10/04)

A general method for the synthesis of 2,4,5-trisubstituted thiazoles has been developed. Starting from commercially available 2-bromothiazole, successive metalations using TMPMgCl?LiCl or TMP2Zn?2MgCl 2?2LiCl lead to the correspondin

Ranging correlated motion (1.5 nm) of two coaxially arranged rotors mediated by helix inversion of a supramolecular transmitter

Hiraoka, Shuichi,Okuno, Erika,Tanaka, Takaaki,Shiro, Motoo,Shionoya, Mitsuhiko

supporting information; experimental part, p. 9089 - 9098 (2009/02/03)

For a long-range transmission of motion between two movable parts apart from each other, transmitters that can precisely correlate these two motions should be properly incorporated into the system. However, such a motional relay is yet to be realized in a

5,6,7,8-tetrahydropyrido[2,3-D]pyrimidines

-

, (2008/06/13)

PCT No. PCT/US96/14822 Sec. 371 Date Feb. 26, 1999 Sec. 102(e) Date Feb. 26, 1999 PCT Filed Sep. 17, 1996 PCT Pub. No. WO97/41115 PCT Pub. Date Nov. 6, 1997Glutamic acid derivatives in which the amino group is substituted with a 2-amino-5,6,7,8-tetrahydro

Cyclopropyl derivative lipoxygenase inhibitors

-

, (2008/06/13)

Certain carbocyclic aryl- and heterocyclic aryl- substituted cyclopropyl N-hydroxyureas, N-hydroxy-carboxamides, and N-acyl-N-hydroxyamines inhibit 5- and/or 12-lipoxygenase and are useful in the treatment of inflammatory disease states.

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