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102170-23-0

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102170-23-0 Usage

General Description

5-hydroxy-6-methylpiperidin-2-one, also known as 6-hydroxy-5-methyl-2-piperidone or N-methylglucinol, is a chemical compound with a molecular formula C6H11NO2. It is a derivative of piperidin-2-one and is classified as an aliphatic amide. 5-hydroxy-6-Methylpiperidin-2-one is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in the manufacture of UV absorbing agents, photographic chemicals, and as a corrosion inhibitor. Additionally, 5-hydroxy-6-methylpiperidin-2-one has been studied for its potential anti-inflammatory and antioxidant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 102170-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,7 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102170-23:
(8*1)+(7*0)+(6*2)+(5*1)+(4*7)+(3*0)+(2*2)+(1*3)=60
60 % 10 = 0
So 102170-23-0 is a valid CAS Registry Number.

102170-23-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-6-methylpiperidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Piperidinone,5-hydroxy-6-methyl

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:102170-23-0 SDS

102170-23-0Downstream Products

102170-23-0Relevant articles and documents

Deoligomerization: a new route to lactams from unsaturated amides via radical oligomerization.

Liu,Wang, Xing,Li, Chaozhong

, p. 361 - 363 (2003)

[reaction: see text] Triethylborane-initiated atom transfer radical oligomerization of N-allyl or N-(3-butenyl)iodoacetamides followed by treatment with hydrochloric acid and subsequent neutralization with K(2)CO(3) led to the formation of the corresponding 5-hydroxyl-substituted delta-lactams or caprolactams, respectively. This oligomerization-deoligomerization sequence serves as an alternative to the corresponding intramolecular cyclization reactions.

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