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9-allyloxy-6-chloro-3-methyl-2,3,4,5-tetrahydro-1H-benzazepine is a complex organic chemical compound with the molecular formula C12H16ClNO. It is a derivative of benzazepine, a class of compounds that are structurally related to benzodiazepines, which are known for their sedative, hypnotic, and anticonvulsant properties. This specific compound features a 6-chloro substitution, a 3-methyl group, and a 9-allyloxy functional group, which contributes to its unique chemical properties. The compound is characterized by its tetrahydro structure, indicating that it has four hydrogen atoms added across the molecule, which can influence its reactivity and stability. It is important to note that while it shares a structural similarity with benzodiazepines, the specific effects and applications of 9-allyloxy-6-chloro-3-methyl-2,3,4,5-tetrahydro-1H-benzazepine may differ and would require further investigation to determine its potential uses and effects.

86120-57-2

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86120-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86120-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,2 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86120-57:
(7*8)+(6*6)+(5*1)+(4*2)+(3*0)+(2*5)+(1*7)=122
122 % 10 = 2
So 86120-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H18ClNO/c1-3-10-17-14-5-4-13(15)11-6-8-16(2)9-7-12(11)14/h3-5H,1,6-10H2,2H3

86120-57-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-3-methyl-9-prop-2-enoxy-2,3,4,5-tetrahydro-1H-1-benzazepine

1.2 Other means of identification

Product number -
Other names 9-(allyloxy)-6-chloro-3-methyl-2,3,4,5-tetrahydro-1H-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:86120-57-2 SDS

86120-57-2Downstream Products

86120-57-2Relevant academic research and scientific papers

6-HALO-9-ALKENYLENEOXY-3-ALKYL-2,3,4,5-TETRAHYDRO-(1H-3)-BENZAZEPINES AND THEIR USE AS SELECTIVE ALPHA-ADRENERGIC RECEPTOR ANTAGONISTS

-

, (2008/06/13)

Selective alpha-adrenoceptor antagonists having the Formula: STR1 which are useful to produce alpha 3-selective adrenoceptor antagonism, pharmaceutical compositions including these antagonists, and methods of using these antagonists to selectively antagonize alpha 3 adrenoceptor mediated activity in mammals.

Development of an affinity ligand for purification of α2-adrenoceptors from human platelet membranes

DeMarinis,Krog,Shah,Lafferty,Holden,Hieble,Matthews,Regan,Lefkowitz,Caron

, p. 918 - 921 (2007/10/02)

Human platelets contain α2-adrenoceptors which are negatively coupled to the enzyme adenylate cyclase. In order to better understand the interaction of this subtype of α receptor with this key enzyme, we have initiated a program to isolate and

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