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

119198-74-2

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119198-74-2 Usage

Chemical compound

5H-Thieno[2,3-c]pyrrole, 5-(phenylmethyl)-

Backbone

thieno[2,3-c]pyrrole

Side chain

phenylmethyl
Heterocyclic compound
Potential pharmacological and therapeutic properties
Studied for potential use as a drug candidate
Potential treatment for cancer and neurological disorders
Unique structure and chemical properties
Promising target for research and development in medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 119198-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,9 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119198-74:
(8*1)+(7*1)+(6*9)+(5*1)+(4*9)+(3*8)+(2*7)+(1*4)=152
152 % 10 = 2
So 119198-74-2 is a valid CAS Registry Number.

119198-74-2SDS

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 5-benzylthieno[2,3-c]pyrrole

1.2 Other means of identification

Product number -
Other names -

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:119198-74-2 SDS

119198-74-2Relevant academic research and scientific papers

Thienopyrroles: Synthesis, Diels-ALder Reaction, and Synthetic Utility

Sha, Chin-Kang,Tsou, Chiu-Peng

, p. 2446 - 2450 (2007/10/02)

5H-Thienopyrrole 1a and the N-substituted derivatives 1b-h and 11-13 were synthesized by the novel retro-malonate addition reaction.Thienopyrroles readily underwent the Diels-Alder reaction with reactive dienophiles, such as N-phenylmaleimid

A Retro-malonate Addition Reaction: Synthesis of 3,4-Condensed Heteroaromatic Pyrroles

Sha, Chin-Kang,Tsou, Chiu-Peng,Li, Yu-Chang,Lee, Ren-Sheng,Tsai, Fu-Yuan,Yeh, Ren-Hwa

, p. 1081 - 1083 (2007/10/02)

Treatment of bromo alkylidenemalonates (1)-(4) with ammonia or amines afforded 3,4-condensed heteroaromatic pyrroles (5)-(8) in excellent yields; benzotripyrroles (19)-(21) were synthesized by the same method.

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