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215033-43-5

1,2,4,5-TETRAHYDROBENZO[D]AZEPINE-3-CARBALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 215033-43-5 Structure

  • Basic information

    1. Product Name: 1,2,4,5-TETRAHYDROBENZO[D]AZEPINE-3-CARBALDEHYDE
    2. Synonyms: 1,2,4,5-TETRAHYDROBENZO[D]AZEPINE-3-CARBALDEHYDE
    3. CAS NO:215033-43-5
    4. Molecular Formula: C11H13NO
    5. Molecular Weight: 175.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215033-43-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2,4,5-TETRAHYDROBENZO[D]AZEPINE-3-CARBALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,4,5-TETRAHYDROBENZO[D]AZEPINE-3-CARBALDEHYDE(215033-43-5)
    11. EPA Substance Registry System: 1,2,4,5-TETRAHYDROBENZO[D]AZEPINE-3-CARBALDEHYDE(215033-43-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 215033-43-5(Hazardous Substances Data)

215033-43-5 Usage

Chemical Class

Benzazepines

Appearance

Yellow to brown crystalline powder

Research and Industry Applications

Pharmaceutical, organic synthesis, chemical intermediate

Potential Medicinal Applications

Building block for the synthesis of novel drugs

Structure

Unique, suitable for creating diverse compounds

Reactivity

Investigated for use in the production of fine chemicals and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 215033-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,0,3 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 215033-43:
(8*2)+(7*1)+(6*5)+(5*0)+(4*3)+(3*3)+(2*4)+(1*3)=85
85 % 10 = 5
So 215033-43-5 is a valid CAS Registry Number.

215033-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,5-tetrahydro-3-benzazepine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1,2,4,5-TETRAHYDROBENZO[D]AZEPINE-3-CARBALDEHYDE

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:215033-43-5 SDS

215033-43-5Relevant articles and documents

7-Endo selective aryl radical cyclization onto enamides leading to 3-benzazepines: Concise construction of a cephalotaxine skeleton

Taniguchi, Tsuyoshi,Ishita, Atsuko,Uchiyama, Masahiko,Tamura, Osamu,Muraoka, Osamu,Tanabe, Genzoh,Ishibashi, Hiroyuki

, p. 1922 - 1925 (2007/10/03)

(Chemical Equation Presented) Bu3SnH-mediated radical cyclizations of 2-(2-bromophenyl)-N-ethenylacetamide gave 6-exo cyclization product 15 as the major product, whereas N-[2-(2-bromophenyl)ethyl]-N- ethenylamides gave almost exclusively 7-end

Thermogenic composition and benzazepine thermogenics

-

, (2008/06/13)

The object of the present invention is to provide a prophylactic and/or therapeutic drug for obesity and obesity-associated diseasestor diabetes with a reduced risk for central side effects and high universality in usage. Another object of the present invention is to provide a pharmaceutical composition comprising a compound of the following formula: wherein Ar represents phenyl which may be substituted and/or condensed; n represents an integer of 1 to 10; R represents hydrogen or a hydrocarbon group which may be substituted, which may not be the same in its n occurrences; R may be bound to either Ar or a substituent for Ar; Y represents an amino group which may be subsituted or a nitrogen-containing saturated heterocyclic group which may be substituted, or a salt thereof, which can be used for a thermogenic agent, an antiobesity agent, a lipolytic agent, or a prophylactic and/or treating drug for obesity-associated diseases.

Preventives and remedies for central nervous system diseases

-

, (2008/06/13)

A prophylactic or therapeutic agent for central nervous system diseases based on amyloid β40 secretion inhibitory activity of a compound having urotensin II receptor antagonistic activity or a salt thereof.

GPR14 ANTAGONIST

-

, (2008/06/13)

A novel GPR14 antagonist. The GPR14 antagonist comprises a compound represented by the formula (I) or a salt thereof wherein Ar represents optionally substituted aryl; X represents a spacer; n is an integer of 1 to 10; R represents an optionally substitut

A synthesis of 2,3,4,5-tetrahydro-1H-3-benzazepines via Pummerer-type cyclization of N-(2-arylethyl)-N-(2-Phenylsulfinylethyl)formamides

Toda, Jun,Ichikawa, Tsuyoshi,Saitoh, Toshiaki,Horiguchi, Yoshie,Sano, Takehiro

, p. 2009 - 2018 (2007/10/03)

A construction of 2,3,4,5-tetrahydro-1H-3-benzazepine ring system (7) was achieved via Pummerer-type cyclization of N-(2-arylethyl)-N-2-(phenylsulfinylethyl)formamides (6). This route produced the benzazepines (10) and (11) in six steps starting from readily available 2-arylethylamines (2) and 2-chloroethyl phenyl sulfide.

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