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73289-66-4

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73289-66-4 Usage

General Description

2-Hydroxy-6-methyl-benzonitrile is a chemical compound with the molecular formula C8H7NO. It is a nitrile derivative with a hydroxyl group and a methyl group attached to a benzene ring. 2-HYDROXY-6-METHYL-BENZONITRILE is commonly used as an intermediate in the synthesis of other organic compounds, including pharmaceuticals and agrochemicals. It is also used in the manufacturing of dyes, perfumes, and other industrial products. 2-Hydroxy-6-methyl-benzonitrile is a colorless to pale yellow liquid with a characteristic odor, and it is considered to be potentially toxic if ingested or inhaled in large quantities. It is important to handle and store this compound with care and follow proper safety protocols when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 73289-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73289-66:
(7*7)+(6*3)+(5*2)+(4*8)+(3*9)+(2*6)+(1*6)=154
154 % 10 = 4
So 73289-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO/c1-6-3-2-4-8(10)7(6)5-9/h2-4,10H,1H3

73289-66-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-6-Methyl-Benzonitrile

1.2 Other means of identification

Product number -
Other names 2-hydroxy-6-methylbenzonitrile

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:73289-66-4 SDS

73289-66-4Downstream Products

73289-66-4Relevant articles and documents

Concise Total Synthesis of Dioncophylline E through an ortho-Arylation Strategy

Toop, Hamish D.,Brusnahan, Jason S.,Morris, Jonathan C.

, p. 8536 - 8538 (2017)

The first total synthesis of the potent antimalarial 7,3′-linked naphthylisoquinoline alkaloid dioncophylline E (1) has been completed. The synthesis proceeds in 12 steps (longest linear sequence) and in 15 % overall yield. Key transformations include an ortho-arylation of a naphthol with an aryllead triacetate to construct the sterically hindered biaryl bond, and a three-step sequence to stereoselectively generate the trans-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline moiety.

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