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10,11-Dihydro-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-ol is a complex organic compound belonging to the class of benzopyridines. It is characterized by a unique molecular structure that features a benzene ring fused to a cyclohepta[b]pyridine ring, with a hydroxyl group attached to the 5-position. 10,11-Dihydro-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-ol is notable for its potential applications in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. Its chemical formula is C14H13NO, indicating the presence of 14 carbon, 13 hydrogen, 1 nitrogen, and 1 oxygen atom. The compound's structure and properties make it a subject of interest for researchers exploring new therapeutic agents and understanding its interactions with biological targets.

17895-95-3

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17895-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17895-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,9 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17895-95:
(7*1)+(6*7)+(5*8)+(4*9)+(3*5)+(2*9)+(1*5)=163
163 % 10 = 3
So 17895-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO/c16-14-11-5-2-1-4-10(11)7-8-13-12(14)6-3-9-15-13/h1-6,9,14,16H,7-8H2

17895-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,11-dihydro-5H-benzo[1,2]cyclohepta[3,4-b]pyridin-11-ol

1.2 Other means of identification

Product number -
Other names 5H-BENZO(4,5)CYCLOHEPTA(1,2-b)PYRIDIN-5-OL,10,11-DIHYDRO

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:17895-95-3 SDS

17895-95-3Downstream Products

17895-95-3Relevant academic research and scientific papers

Cyclizations of phenylethyl-substituted pyridinecarboxaldehydes

Naredla, Rajasekhar Reddy,Klumpp, Douglas A.

, p. 2137 - 2141 (2013/03/14)

Several phenylethyl-substituted pyridinecarboxaldehydes were prepared from 2-bromo-3-pyridine-carboxaldehyde and these substances are found to undergo cyclization reactions in acidic media. In the absence of added nucleophile, acid-promoted cyclization and oxidation (MnO2) provide an efficient route to 10,11-dihydro-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-ones. Arene nucleophiles may also be added to the acidic mixture to provide good yields of triarylmethane products. Mechanisms are proposed involving dicationic superelectrophilic intermediates.

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