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34840-23-8

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34840-23-8 Usage

Description

1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudourea is a thiourea derivative, which is an organic compound characterized by the presence of a thiocarbonyl group (C=S) instead of a carbonyl group (C=O) in its structure. 1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudoeura is known for its potential applications in various chemical syntheses and pharmaceutical development.

Uses

1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudourea is used as an intermediate in the synthesis of various compounds for different purposes. The expression is: 1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudourea is used as [application type] for [application reason]
Used in Pharmaceutical Synthesis:
1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudourea is used as a key intermediate in the synthesis of pharmaceutical compounds, such as:
1. Methyl (6-methyl-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-2-yl)carbamate: 1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudoeura is synthesized for its potential applications in the development of new drugs targeting various diseases.
2. 2-amino-5-benzyl-6-methyl-3,5-dihydro-4H-pyrrolo[3,2-d]pyrimidin-4-one: This molecule is synthesized for its potential use in the creation of novel therapeutic agents.
3. Methyl-5-[(3-hydroxypropyl)thio]-1H-benzo[d]imidazol-2-ylcarbamate (hydroxyalbendazole): 1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudoeura is synthesized for its potential applications in the treatment of parasitic infections.
4. Methyl-5-[(4-hydroxyphenyl)thio]-1H-benzo[d]imidazol-2-yl carbamate (hydroxyfenbendazole): This molecule is synthesized for its potential use in the development of new anthelmintic drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 34840-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,4 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34840-23:
(7*3)+(6*4)+(5*8)+(4*4)+(3*0)+(2*2)+(1*3)=108
108 % 10 = 8
So 34840-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O4S/c1-11-5(9)7-4(13-3)8-6(10)12-2/h1-3H3,(H,7,8,9,10)

34840-23-8 Well-known Company Product Price

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  • Aldrich

  • (466476)  1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudourea  97%

  • 34840-23-8

  • 466476-5G

  • 728.91CNY

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34840-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudoeura

1.2 Other means of identification

Product number -
Other names 2-Methylisothiourea-1,3-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:34840-23-8 SDS

34840-23-8Relevant articles and documents

PYRAZOLE-OXAZOLIDINONE COMPOUND FOR ANTI-HEPATITIS B VIRUS

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Paragraph 0397-0399, (2019/06/07)

The present invention discloses a pyrazole-oxazolidinone compound having anti-hepatitis B virus activity, which has the structure of formula (I), wherein each variable is as defined herein.

Process for the preparation of 9-deazaguanine derivatives

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Page 16, (2010/02/09)

Derivatives of 9-deazaguanine are prepared by reacting an aldehyde or ketone with a dialkylaminomalonate to form the corresponding enamine. The enamine is then reacted with a base to form a cyclic pyrrole. The cyclic pyrrole is reacted with an urea compound or a derivative of carbamimidoic acid to provide a protected guanidino compound. The guanidino is converted to the desired 9-deazaguanine derivative by reacting with trifluoracetic acid or with an alkoxide or hydroxide followed by neutralization with an acid.

Process for the preparation of 9-deazaguanine derivatives

-

, (2008/06/13)

Derivatives of 9-deazaguanine are prepared by reacting an aldehyde or ketone with a dialkylaminomalonate to form the corresponding enamine. The enamine is then reacted with a base to form a cyclic pyrrole. The cyclic pyrrole is reacted with an urea compound to provide a protected guanidino compound. The guanidino is converted to the desired 9-deazaguanine derivative by reacting with trifluoracetic acid or with an alkoxide or hydroxide followed by neutralization with an acid.

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