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2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPIN-7-OL, also known as tetrahydrobenzo[d]azepin-7-ol, is a bicyclic compound that features a six-membered benzene ring and a seven-membered nitrogen-containing ring. It is recognized for its potent psychoactive properties and has demonstrated sedative, anxiolytic, and antipsychotic effects. As a serotonin receptor antagonist, 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPIN-7-OL has been investigated for its potential role in treating anxiety, depression, and psychotic disorders. It also shows promise in modulating neurotransmitter levels, particularly serotonin and norepinephrine, which may provide therapeutic benefits for mood and anxiety disorders. However, due to its psychoactive nature, it is crucial to use 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPIN-7-OL under the supervision of a healthcare professional.

36133-00-3

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36133-00-3 Usage

Uses

Used in Pharmaceutical Industry:
2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPIN-7-OL is used as a psychoactive substance for its potential therapeutic effects in treating anxiety, depression, and psychotic disorders. Its anxiolytic, sedative, and antipsychotic properties make it a candidate for further research and development in the field of mental health.
Used in Neurotransmitter Modulation:
2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPIN-7-OL is used as a modulator of neurotransmitter levels, particularly serotonin and norepinephrine, to potentially offer therapeutic benefits in mood and anxiety disorders. Its ability to influence these neurotransmitters suggests its potential use in the development of medications targeting neurochemical imbalances.

Check Digit Verification of cas no

The CAS Registry Mumber 36133-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,3 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36133-00:
(7*3)+(6*6)+(5*1)+(4*3)+(3*3)+(2*0)+(1*0)=83
83 % 10 = 3
So 36133-00-3 is a valid CAS Registry Number.

36133-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5-Tetrahydro-1H-3-benzazepin-7-ol

1.2 Other means of identification

Product number -
Other names 7-hydroxy-1H-2,3,4,5-tetrahydro-3-benzazepine

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:36133-00-3 SDS

36133-00-3Relevant academic research and scientific papers

TETRAHYDRO-BENZOAZEPINE GLYCOSIDASE INHIBITORS

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Page/Page column 136, (2020/03/15)

Compounds of formula (I') wherein A, R1, R2, T1, T2, T3, T4, L, W, Z, R''', m and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

Tetrahydro-3-benzazepines with fluorinated side chains as NMDA and σ1 receptor antagonists: Synthesis, receptor affinity, selectivity and antiallodynic activity

Thum, Simone,Schepmann, Dirk,Ayet, Eva,Pujol, Marta,Nieto, Francisco R.,Ametamey, Simon M.,Wünsch, Bernhard

supporting information, p. 47 - 62 (2019/05/27)

The class of tetrahydro-1H-3-benzazepines was systematically modified in 1-, 3- and 7-position. In particular, a F-atom was introduced in β- or γ-position of the 4-phenylbutyl side chain in 3-position. Ligands with the F-atom in γ-position possess higher

Synthesis and biological evaluation of N-alkylated 8-oxybenz[c]azepine derivatives as selective PPARδ agonists

Luckhurst, Christopher A.,Ratcliffe, Marianne,Stein, Linda,Furber, Mark,Botterell, Sara,Laughton, David,Tomlinson, Wendy,Weaver, Richard,Chohan, Kamaldeep,Walding, Andrew

scheme or table, p. 531 - 536 (2011/02/27)

We describe the discovery of small molecule benzazepine derivatives as agonists of human peroxisome proliferator-activated receptor δ (PPARδ) that displayed excellent selectivity over the PPARα and PPARγ subtypes. Compound 8 displayed good PK in the rat a

COMPOUNDS HAVING AFFINITY FOR THE DOPAMINE D3 RECEPTOR AND USES THEREOF IN MEDICINE

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Page/Page column 22, (2010/02/15)

Compounds of formula (I) or a salt thereof are disclosed, wherein A, m R1, R2, R3, q, W1, W2, R4 and R5 are as defined in the description. Processes for preparation and uses of the compounds in medicine, for example for the treatment of schizophrenia or drug dependency, are also disclosed.

DOPAMINE RECEPTOR MODULATORS AS ANTIPSYCHOTIC AGENTS

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Page/Page column 25, (2010/02/07)

The invention provides compounds of formula (I):wherein A and B represent the groups -(CH2)m- and -(CH2)n-respectively; R1 represents hydrogen or C1-6alkyl; R2 represents hydroge

Novel 2,3,4,5-tetrahydro-1H-3-benzazepines with high affinity and selectivity for the dopamine D3 receptor

Austin, Nigel E.,Avenell, Kim Y.,Boyfield, Izzy,Branch, Clive L.,Hadley, Michael S.,Jeffrey, Phillip,Johnson, Christopher N.,Macdonald, Gregor J.,Nash, David J.,Riley, Graham J.,Smith, Alexander B.,Stemp, Geoffrey,Thewlis, Kevin M.,Vong, Antonio K. K.,Wood, Martyn

, p. 2553 - 2555 (2007/10/03)

Starting from the dopamine D3 receptor antagonist SB-277011 1, a series of 2,3,4,5-tetrahydro-1H-3-benzazepines has been identified with high affinity for the dopamine D3 receptor and selectivity over the D2 receptor. The 3-acetamido-2-fluorocinnamide derivative 20 gave high D3 receptor affinity (pK(i) 8.4) with 130-fold selectivity over the D2 receptor. (C) 2000 Elsevier Science Ltd.

2-pyrrolidinones, pharmaceutical compositions containing these compounds and processes for preparing them

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, (2008/06/13)

The invention relates to cyclic imino derivatives of general formula wherein A, B, E, X2 to X5 and Y are defined as in claim 1, the stereoisomers, tautomers, mixtures and salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, which have valuable pharmacological properties, preferably aggregation-inhibiting effects, pharmaceutical compositions which contain these compounds and processes for preparing them.

Substituted 1,2,4,5-tetrahydro-3H,3 benzazepines

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, (2008/06/13)

Compounds of the general formula: STR1 and pharmaceutical acceptable salts thereof wherein R is H, lower alkyl, lower alkenyl, lower aralkenyl, cycloalkyl-alkyl, propargyl, lower aralkyl, hydroxyalkyl and esters thereof, heterocyclic, heterocyclic-alkyl,

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