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81094-63-5

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81094-63-5 Usage

General Description

1,4,5,6-tetrahydro-3H-1,5-methano-2,4-benzoxazocin-3-one is a chemical compound with a complex molecular structure. It belongs to the family of benzoxazocin-3-one derivatives and is primarily used in medicinal chemistry for research purposes. 1,4,5,6-tetrahydro-3H-1,5-methano-2,4-benzoxazocin-3-one has shown potential in the development of new pharmaceutical drugs, particularly in the fields of neuroscience and psychiatry. Its unique structure and pharmacological properties make it an interesting target for further investigation and potential drug development. However, due to its complex nature, further research is needed to fully understand its potential applications and therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 81094-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,9 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81094-63:
(7*8)+(6*1)+(5*0)+(4*9)+(3*4)+(2*6)+(1*3)=125
125 % 10 = 5
So 81094-63-5 is a valid CAS Registry Number.

81094-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,5,6-tetrahydro-1,5-methano-2,4-benzoxazecin-3-one

1.2 Other means of identification

Product number -
Other names 1,4,5,6-TETRAHYDRO-1,5-METHANO-3H-2,4-BENZOXAZOCIN-3-ONE

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:81094-63-5 SDS

81094-63-5Downstream Products

81094-63-5Relevant articles and documents

A new, potent, conformationally restricted analogue of amphetamine: 2-Amino-1,2-dihydronapthalene

Hathaway,Nichols,Nichols,Yim

, p. 535 - 538 (1982)

A new stimulant compound, 1,2-dihydro-2-naphthalenamine (2-amino-1,2-dihydronaphthalene, 2-ADN), was prepared as an analogue of amphetamine and of 2-aminotetralin. The optical isomers of 2-ADN were obtained by chemical resolution, and the absolute configuration was determined to be R-(+) and S-(-). Preliminary pharmacological evaluation revealed that racemic 2-ADN is approximately one-fourth as potent as (+)-amphetamine as a stimulant in mice. The S-(-) isomer of 2-ADN was found to be solely responsible for the stimulant effects of the racemate. Both reserpine and α-methyl-p-tyrosine antagonized the stimulation produced by 2-ADN.

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