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Pentanamide, N-hydroxy-4-methyl-, also known as N-hydroxy-4-methylpentanamide, is an organic compound with the chemical formula C6H13NO2. It is a derivative of pentanamide, featuring a hydroxyl group (-OH) and a methyl group (-CH3) attached to the nitrogen atom. Pentanamide, N-hydroxy-4-methyl- is a colorless liquid with a molecular weight of 131.17 g/mol. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is essential to handle Pentanamide, N-hydroxy-4-methyl- with care, following proper safety protocols and guidelines.

4132-36-9

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4132-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4132-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,3 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4132-36:
(6*4)+(5*1)+(4*3)+(3*2)+(2*3)+(1*6)=59
59 % 10 = 9
So 4132-36-9 is a valid CAS Registry Number.

4132-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Methyl-valeryl)-hydroxylamin

1.2 Other means of identification

Product number -
Other names N-HYDROXY-4-METHYLPENTANAMIDE

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:4132-36-9 SDS

4132-36-9Relevant academic research and scientific papers

Strategic Approach to the Metamorphosis of γ-Lactones to NH γ-Lactams via Reductive Cleavage and C-H Amidation

Jung, Hoi-Yun,Chang, Sukbok,Hong, Sungwoo

, p. 7099 - 7103 (2019)

A new approach has elaborated on the conversion of γ-lactones to the corresponding NH γ-lactams that can serve as γ-lactone bioisosteres. This approach consists of reductive C-O cleavage and an Ir-catalyzed C-H amidation, offering a powerful synthetic tool for accessing a wide range of valuable NH γ-lactam building blocks starting from γ-lactones. The synthetic utility was further demonstrated by the late-stage transformation of complex bioactive molecules and the asymmetric transformation.

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