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6-Butyl-6,7-dihydro-5H-dibenz[c,e]azepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58335-96-9

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58335-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58335-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,3 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58335-96:
(7*5)+(6*8)+(5*3)+(4*3)+(3*5)+(2*9)+(1*6)=149
149 % 10 = 9
So 58335-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H21N/c1-2-3-12-19-13-15-8-4-6-10-17(15)18-11-7-5-9-16(18)14-19/h4-11H,2-3,12-14H2,1H3

58335-96-9SDS

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 6-n-butyl-6,7-dihydro-5H-dibenz[c,e]azepine

1.2 Other means of identification

Product number -
Other names 6-butyl-6,7-dihydro-5H-dibenz[c,e]azepine

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:58335-96-9 SDS

58335-96-9Downstream Products

58335-96-9Relevant academic research and scientific papers

Intramolecular C(sp3)-N coupling by oxidation of benzylic C,N-dianions

Jeffrey, Jenna L.,Bartlett, Emily S.,Sarpong, Richmond

, p. 2194 - 2197 (2013/03/28)

What a couple! An intramolecular, C(sp3)-N coupling to afford azacycles is reported. This reaction proceeds through the oxidation of benzylic C,N-dianions with iodine and builds on an earlier discovery during the synthesis of the natural produc

A facile synthesis of 6-alkyl-6,7-dihydro-5H-dibenz[c,e]azepines: Potent hypolipidemics

Akula,Kabalka

, p. 3901 - 3906 (2007/10/03)

6-Alkyl-6,7-dihydro-5H-dibenz[c,e]azepines were synthesized in two steps in 63-88% overall yield by utilizing an efficient borane-tetrahydrofuran reduction of imides.

Hypolipidemic activity of 6-substituted 6,7-dihydro-5H-dibenz[c,e]azepine and the effects of 6,7-dihydro-5H-dibenz[c,e]azepine on lipid metabolism of rodents

Hall,Murthy,Wyrick

, p. 622 - 626 (2007/10/02)

A series of 6-substituted derivatives of 6,7-dihydro-5H-dibenz[c,e]azepine was found to be active hypolipidemic agents in rodents at doses of mg/kg per day. The parent drug was found to suppress the enzyme activity of ATP-dependent citrate lyase, sn-glyce

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