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6530-36-5

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6530-36-5 Usage

General Description

Isonicotinaldehyde O-benzyloxime is a chemical compound with the molecular formula C13H11NO2. It is an organic compound that belongs to the class of aldehydes and isonicotinaldehyde derivatives. isonicotinaldehyde O-benzyloxime has a benzyl group attached to the oxygen atom in the oxime functional group, giving it a unique structure and properties. Isonicotinaldehyde O-benzyloxime has potential applications in organic synthesis and pharmaceutical research due to its reactivity and ability to undergo various chemical reactions. Additionally, it may also be used as a building block in the synthesis of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 6530-36-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6530-36:
(6*6)+(5*5)+(4*3)+(3*0)+(2*3)+(1*6)=85
85 % 10 = 5
So 6530-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O/c1-2-4-13(5-3-1)11-16-15-10-12-6-8-14-9-7-12/h1-10H,11H2

6530-36-5SDS

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 N-phenylmethoxy-1-pyridin-4-ylmethanimine

1.2 Other means of identification

Product number -
Other names Pyridin-aldehyd-(4)-<O-benzyl-oxim>

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:6530-36-5 SDS

6530-36-5Downstream Products

6530-36-5Relevant articles and documents

Metal-Free Transformation of Sulfonyl Oxime Ethers with Amines to Oxime Ethers

Zhang, Jia-Yuan,Hu, Jinglin,Li, Xiao-Xuan,Tang, Wei-Ke,Feng, Yi-Si

, p. 12676 - 12682 (2021/09/18)

Sulfonyl oxime ethers undergo facile radical substitutions with various amines to yield the corresponding oxime ethers. An efficient arylation of sulfonyl oxime ethers was accomplished under ambient temperature and metal-free conditions, with a wide range of functional group tolerance. Mechanistic investigations indicate that a phenyl radical is involved in the catalytic cycle.

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