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1H-Thieno[3,4-c]pyrrole, 3,4,5,6-tetrahydro-5-(phenylmethyl)-, 2,2-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35105-74-9

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35105-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35105-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,0 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35105-74:
(7*3)+(6*5)+(5*1)+(4*0)+(3*5)+(2*7)+(1*4)=89
89 % 10 = 9
So 35105-74-9 is a valid CAS Registry Number.

35105-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzyl-3,4,5,6-tetrahydro-1H-thieno[3,4-c]pyrrole 2,2-dioxide

1.2 Other means of identification

Product number -
Other names 5-Benzyl-3,4,5,6-tetrahydro-1H-thieno[3,4-c]pyrrole 2,2-dioxide

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:35105-74-9 SDS

35105-74-9Relevant academic research and scientific papers

2-PHENYL-5-HETEROCYCLYL-TETRAHYDRO-2H-PYRAN-3-AMINE COMPOUNDS FOR USE IN THE TREATMENT OF DIABETES AND ITS ASSOCIATED DISORDERS

-

, (2014/05/07)

The present invention relates to novel compounds of the general formula (I) their tautomeric forms, their enantiomers, their diastereoisomers, their pharmaceutically accepted salts, or pro-drugs thereof, which are useful for the treatment or prevention of diabetes mellitus (DM), obesity and other metabolic disorders. The invention also relates to process for the manufacture of said compounds, and pharmaceutical compositions containing them and their use.

New Building Blocks, 3,5-Dihydro-1H-thienopyrrole 2,2-Dioxides; Preparation and their Diels-Alder Reaction with Dimethyl Acetylenedicarboxylate

Ando, Kaori,Kankake, Mutsuo,Suzuki, Takayoshi,Takayama, Hiroaki

, p. 129 - 138 (2007/10/02)

New building blocks, 3,5-dihydro-1H-thienopyrrole 2,2-dioxides 3, have been prepared by the oxidation of their corresponding pyrroline derivates 4 with DDQ or Chemical MnO2.The Diels-Alder reaction of 3 with dimethyl acetylenedicarboxylate gave new types of compounds: 7-aza-2,3-dimethylenenorbornenes A, the 1:2 adducts B, 1a,3a,6,9-tetrahydrobenzindoles C, and dihydroindolosulfolene D depending on the reaction conditions and the N-substituents.The reaction of 3 with bis(tert-butylsulfonyl)acetylene was also described.

New Building Blocks, 3,5-Dihydro-1H-thienopyrrole 2,2-Dioxides; Preparation and their Diels-Alder Reaction with Dimethyl Acetylenedicarboxylate

Ando, Kaori,Kankake, Mutuo,Suzuki, Takayoshi,Takayama, Hiroaki

, p. 1100 - 1102 (2007/10/02)

New building blocks, 3,5-dihydro-1H-thienopyrrole 2,2-dioxides 1, have been prepared and react with dimethyl acetylenedicarboxylate to give new types of compound; 7-aza-2,3-dimethylenenorbornene A, the 1 : 2 adduct B, 1a,3a,6,9-tetrahydrobenzindole C, and dihydroindolosulfolene D depending on the reaction conditions and the N-substituent.

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