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204691-99-6

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204691-99-6 Usage

General Description

4-Benzamido-cyclohexanol is a chemical compound with the molecular formula C13H17NO2. It is a white solid that is sparingly soluble in water and has a melting point of 124-126°C. 4-Benzamido-cyclohexanol is commonly used as a reagent in organic synthesis and pharmaceutical research. It is known for its ability to act as a chiral auxiliary in the asymmetric synthesis of various organic compounds. Additionally, 4-Benzamido-cyclohexanol has been studied for its potential pharmacological activities, particularly as an analgesic and anti-inflammatory agent. Its unique structure and versatile reactivity make it a valuable chemical in the fields of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 204691-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,6,9 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 204691-99:
(8*2)+(7*0)+(6*4)+(5*6)+(4*9)+(3*1)+(2*9)+(1*9)=136
136 % 10 = 6
So 204691-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO2/c15-12-8-6-11(7-9-12)14-13(16)10-4-2-1-3-5-10/h1-5,11-12,15H,6-9H2,(H,14,16)

204691-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-hydroxycyclohexyl)benzamide

1.2 Other means of identification

Product number -
Other names N-(4-oxidanylcyclohexyl)benzamide

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:204691-99-6 SDS

204691-99-6Relevant articles and documents

N-heterocyclic carbene-catalyzed oxidative amidation of aldehydes with amines

Alanthadka, Anitha,Maheswari, C. Uma

supporting information, p. 1199 - 1203 (2015/04/22)

The N-heterocyclic carbene (NHC)-catalyzed oxidative amidation of aromatic aldehydes with amines in the presence of N-bromosuccinimide (NBS) as an oxidant has been developed for the synthesis of amides. This amidation strategy is tolerant to both the electronic and the steric nature of the aryl aldehydes employed. The present methodology was extended to chiral amino acid derivatives to generate the corresponding amides in good yields and excellent ee values (>98%).

Synthesis and microbial hydroxylation of some azabicycloalkanes

Olivo, Horacio F.,Hemenway, Michael S.,Gezginci, Mikail H.

, p. 1309 - 1312 (2007/10/03)

N-Substituted 7-azabicyclo[2.2.1]heptanes have been synthesized in a short route. These compounds containing benzamide or benzenesulfonamide groups are good substrates for microbial oxidation of unactivated carbons by B. bassiana.

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