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N-(9-Anthracenylmethyl)cinchonindinium chloride is a synthetic organic compound derived from the natural alkaloid cinchonidine. It is characterized by its unique chemical structure, which includes an anthracenylmethyl group attached to the cinchonindinium framework. N-(9-ANTHRACENYLMETHYL)CINCHONINDINIUMCHLORIDE is known for its potential applications in the field of asymmetric catalysis and as a chiral phase-transfer catalyst.

199588-80-2

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199588-80-2 Usage

Uses

1. Used in Asymmetric Catalysis:
N-(9-Anthracenylmethyl)cinchonindinium chloride is used as a chiral catalyst in asymmetric catalysis for enhancing the enantioselectivity of various chemical reactions. Its unique structure allows it to interact with substrates in a stereospecific manner, leading to the formation of chiral products with high enantiomeric excess.
2. Used in the Preparation of Chiral Phase-Transfer Catalysts:
N-(9-Anthracenylmethyl)cinchonindinium chloride is used as a precursor in the synthesis of O-allyl-N-(9-anthracenylmethyl)cinchonidinium bromide, a cinchona-based chiral phase-transfer catalyst (PTC). These PTCs are valuable in promoting a wide range of organic reactions, such as alkylation, acylation, and cyclopropanation, with high enantioselectivity.
3. Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(9-Anthracenylmethyl)cinchonindinium chloride may find applications in the development of novel drugs with improved chiral selectivity. Its ability to act as a chiral catalyst can be harnessed to synthesize enantiomerically pure drug candidates, which is crucial for ensuring the desired therapeutic effects and minimizing potential side effects.
4. Used in Chemical Research:
N-(9-Anthracenylmethyl)cinchonindinium chloride can be employed as a research tool in the field of organic chemistry, particularly in the study of asymmetric catalysis and the development of new chiral catalysts. Its unique structure and reactivity make it an interesting candidate for exploring new reaction mechanisms and designing innovative synthetic routes.

Check Digit Verification of cas no

The CAS Registry Mumber 199588-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,5,8 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 199588-80:
(8*1)+(7*9)+(6*9)+(5*5)+(4*8)+(3*8)+(2*8)+(1*0)=222
222 % 10 = 2
So 199588-80-2 is a valid CAS Registry Number.

199588-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(anthracen-9-ylmethyl)-5-ethenyl-1-azoniabicyclo[2.2.2]octan-2-yl]-quinolin-4-ylmethanol,chloride

1.2 Other means of identification

Product number -
Other names -

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:199588-80-2 SDS

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