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175136-34-2

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175136-34-2 Usage

Description

3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-AMINE is an organic compound that serves as a crucial intermediate in various chemical and pharmaceutical processes. Its unique chemical structure allows it to be a versatile building block for the synthesis of different compounds.

Uses

Used in Organic Synthesis:
3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-AMINE is used as a key intermediate for the synthesis of various organic compounds. Its chemical reactivity and structural properties make it a valuable component in the creation of a wide range of molecules.
Used in Pharmaceutical Industry:
3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-AMINE is used as a vital building block in the development of new pharmaceuticals. Its incorporation into drug molecules can potentially enhance their efficacy, selectivity, and pharmacokinetic properties.
Used in Agrochemicals:
In the agrochemical industry, 3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-AMINE is used as a starting material for the synthesis of various agrochemical products. Its presence in these compounds can contribute to their effectiveness in protecting crops and improving agricultural yields.
Used in Dye Industry:
3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-AMINE is also utilized in the dye industry as a raw material for the production of different types of dyes. Its chemical structure can be manipulated to create dyes with specific color properties and stability, catering to various applications in textiles, plastics, and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 175136-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175136-34:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*6)+(2*3)+(1*4)=132
132 % 10 = 2
So 175136-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c10-7-2-3-8-9(6-7)12-5-1-4-11-8/h2-3,6H,1,4-5,10H2

175136-34-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H27862)  3,4-Dihydro-2H-1,5-benzodioxepin-7-amine, 98%   

  • 175136-34-2

  • 1g

  • 704.0CNY

  • Detail
  • Alfa Aesar

  • (H27862)  3,4-Dihydro-2H-1,5-benzodioxepin-7-amine, 98%   

  • 175136-34-2

  • 5g

  • 2147.0CNY

  • Detail

175136-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-AMINE

1.2 Other means of identification

Product number -
Other names 3,4-dihydro-7-amino-2H-1,5-benzo[b][1,4]dioxepin

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:175136-34-2 SDS

175136-34-2Downstream Products

175136-34-2Relevant articles and documents

Guanidine compound for preventing and treating chronic pain medication (by machine translation)

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, (2020/08/27)

The invention relates to a guanidine compound as shown in general formula (I) as a guanidine compound for preventing and treating chronic pain disease. A pharmaceutically acceptable salt thereof, a prodrug thereof, a solvate thereof, a deuterated substanc

Exploring Epidermal Growth Factor Receptor (EGFR) inhibitor features: The role of fused dioxygenated rings on the quinazoline scaffold

Chilin, Adriana,Conconi, Maria Teresa,Marzaro, Giovanni,Guiotto, Adriano,Urbani, Luca,Tonus, Francesca,Parnigotto, Pierpaolo

supporting information; experimental part, p. 1862 - 1866 (2010/08/06)

A number of dioxolane, dioxane, and dioxepine quinazoline derivatives have been synthetized, and evaluated as EGFR inhibitors. Their cytotoxic activity has been tested against two cell, lines overexpressing and not expressing EGFR. Most derivatives were a

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