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55267-92-0

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55267-92-0 Usage

General Description

1-(6-methylpiperidin-2-yl)propan-2-ol is a chemical compound with the molecular formula C10H21NO. It is an alcohol derivative containing a piperidine ring and a methyl group attached to the nitrogen atom. 1-(6-methylpiperidin-2-yl)propan-2-ol is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It can be produced through various chemical reactions, and its properties make it suitable for use in the pharmaceutical and chemical industries. The compound may have potential applications in drug development and other fields due to its unique structural features. Overall, 1-(6-methylpiperidin-2-yl)propan-2-ol is an important molecule with potential implications in various scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 55267-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55267-92:
(7*5)+(6*5)+(5*2)+(4*6)+(3*7)+(2*9)+(1*2)=140
140 % 10 = 0
So 55267-92-0 is a valid CAS Registry Number.

55267-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-methylpiperidin-2-yl)propan-2-ol,hydrochloride

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:55267-92-0 SDS

55267-92-0Upstream product

55267-92-0Downstream Products

55267-92-0Relevant articles and documents

N-sulfinyl amines as a nitrogen source in the asymmetric intramolecular aza-michael reaction: Total synthesis of (-)-pinidinol

Fustero, Santos,Monteagudo, Silvia,Sanchez-Rosello, Maria,Flores, Sonia,Barrio, Pablo,Del Pozo, Carlos

supporting information; experimental part, p. 9835 - 9845 (2010/10/19)

N-Sulfinyl amines have been successfully employed as nitrogen nucleophiles for the asymmetric intramolecular aza-Michael reaction. The synthetic strategy involves a cross-metathesis reaction followed by the Michael-type cyclization, either in a base-catalyzed two-step procedure or in a tandem fashion. The developed methodology allows access to chiral substituted pyrrolidines and piperidines bearing one or two stereocenters and it has been applied to the synthesis of the piperidine alkaloid (-)-pinidinol.

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