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(3aR,12R,12aR,12bS)-12-amino-10-hydroxy-2,3,3a,4,11,12,12a,12b-octahydroisoquino[2,1,8-lma]carbazol-5(1H)-one hydrochloride (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133775-36-7

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133775-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133775-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,7 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133775-36:
(8*1)+(7*3)+(6*3)+(5*7)+(4*7)+(3*5)+(2*3)+(1*6)=137
137 % 10 = 7
So 133775-36-7 is a valid CAS Registry Number.

133775-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name <3aR-(3aα,12α,12aα,12bα)>-12-amino-2,3,3a,4,11,12,12a,12b-octahydro-10-hydroxyisoquino<2,1,8-lma>carbazol-2(1H)-one hydrochloride

1.2 Other means of identification

Product number -
Other names (3aR,12R,12aR,12bS)-12-amino-2,3,3a,4,11,12,12a,12b-octahydro-10-hydroxyisoquino<2,1,8-lma>carbazol-5(1H)-one hydrochloride

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:133775-36-7 SDS

133775-36-7Relevant academic research and scientific papers

Synthesis of an enantiomerically pure aminoisoquinocarbazole with antiarrhythmic activity via lipase-catalyzed enantioselective transesterification

Fukazawa, Tetuya,Shimoji, Yasuo,Hashimoto, Toshihiko

, p. 1649 - 1658 (2007/10/03)

Enantiomerically pure (R)-2-cyclohexen-1-ol 5 was prepared via lipase- catalyzed enantioselective transesterification of 2-substituted cyclohexanol, and stereospecifically converted to (-)-(2-cyclohexenyl)acetic acid 4. Enantiomerically pure aminoisoquinocarbazole 1 (RS-2135) was synthesized stereoselectively from 4, using an intramolecular Diels-Alder reaction and Curtius rearrangement.

Synthesis and biological action of the aminotetrahydroisoquinocarbazoles and related compounds: A new class of compounds with antiarrhythmic activity

Shimoji,Tomita,Hashimoto,Saito,Morisawa,Mizuno,Yorikane,Koike

, p. 816 - 822 (2007/10/02)

A series of 12-aminotetrahydroisoquinocarbazoles and related compounds were synthesized using an intramolecular Diels-Alder reaction and screened for antiarrhythmic activity in chloroform-induced ventricular arrhythmias in mice. Several compounds showed m

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