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1196075-55-4

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1196075-55-4 Usage

General Description

Di-tert-butyl 3,4-dihydro-1H-pyrido[3,4-b]indole-2,9-dicarboxylate is a chemical compound with the molecular formula C24H32N2O4. It is a synthetic derivative of the alkaloid yohimbine and has potential pharmaceutical applications. The compound is an ester, and its tert-butyl groups provide steric hindrance, making it less reactive than other similar compounds. Di-tert-butyl 3,4-dihydro-1H-pyrido[3,4-b]indole-2,9-dicarboxylate may have potential uses in the field of medicinal chemistry and drug development due to its unique structure and properties. Further research is needed to fully understand its potential applications and implications.

Check Digit Verification of cas no

The CAS Registry Mumber 1196075-55-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,0,7 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1196075-55:
(9*1)+(8*1)+(7*9)+(6*6)+(5*0)+(4*7)+(3*5)+(2*5)+(1*5)=174
174 % 10 = 4
So 1196075-55-4 is a valid CAS Registry Number.

1196075-55-4SDS

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 ditert-butyl 3,4-dihydro-1H-pyrido[3,4-b]indole-2,9-dicarboxylate

1.2 Other means of identification

Product number -
Other names QC-4506

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:1196075-55-4 SDS

1196075-55-4Downstream Products

1196075-55-4Relevant articles and documents

Catalytic Enantioselective Synthesis of Spirooxindoles by Oxidative Rearrangement of Indoles

Qian, Chenxiao,Li, Pengfei,Sun, Jianwei

, p. 5871 - 5875 (2021)

Oxidative rearrangement of indoles to access oxindoles has been used as a key step in complex molecule synthesis. We report a catalytic enantioselective variant of this transformation by chiral phosphoric acid catalysis, providing rapid access to a range of enantioenriched spirooxindoles. The high enantioselectivity is controlled by dynamic kinetic resolution.

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