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7-METHOXY-4-METHYLINDAN-1-ONE is a chemical compound belonging to the indanone class, characterized by its white to light yellow solid appearance and a molecular formula of C11H12O2. It is known for its unique structure and reactivity, which makes it a versatile component in various applications.

67901-83-1

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67901-83-1 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
7-METHOXY-4-METHYLINDAN-1-ONE is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity, contributing to the development of new drugs and pesticides.
Used in Medicinal Applications:
7-METHOXY-4-METHYLINDAN-1-ONE is used as a potential medicinal compound for its anti-inflammatory and analgesic effects, indicating its potential in the treatment of pain and inflammation.
Used in Fragrance Industry:
7-METHOXY-4-METHYLINDAN-1-ONE is used as a fragrance ingredient in perfumes and personal care products, leveraging its aromatic properties to enhance the scent profiles of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 67901-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,0 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67901-83:
(7*6)+(6*7)+(5*9)+(4*0)+(3*1)+(2*8)+(1*3)=151
151 % 10 = 1
So 67901-83-1 is a valid CAS Registry Number.

67901-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methoxy-4-methyl-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 7-Methoxy-4-Methyl-1-indanon

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:67901-83-1 SDS

67901-83-1Relevant academic research and scientific papers

Synthesis and molecular structure of D-Homo-B-nor-8α analogs of steroidal estrogens

Shavva,Antimonova,Baigozin,Starova,Selivanov,Morozkina

experimental part, p. 1511 - 1516 (2011/02/25)

According to the X-ray diffraction and NMR data, two D-homo-B-nor-8α- analogs of steroidal estrogens in crystal and in solution have similar conformations. The distances between hydrogen atoms in their molecules, calculated ab initio and by the PM3 and MM

The Dimerisation of Some 4-Hydroxyindenes

Davis, Brian R.,Johnson, Stephen J.,Woodgate, Paul D.

, p. 2545 - 2554 (2007/10/02)

The acid-catalysed dimerisation of the indenes (1)-(5), has been studied and a number of products isolated.The structure and stereochemistry of these compounds has been established by the use of crossed dimers, 13C-labelling, and 1H and 13C n.m.r. spectroscopy.

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