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58920-75-5

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58920-75-5 Usage

Physical appearance

It is a yellow to brownish crystalline solid.

Melting point

2,2-diacetyl-indane has a melting point of approximately 81-85 degrees Celsius.

Usage

It is commonly used as a fragrance and flavoring agent in various consumer products, such as perfumes, candles, and air fresheners.

Odor

2,2-diacetyl-indane is known for its sweet, floral, and fruity odor.

Purpose

It is often used to impart a pleasant scent to personal care and household products.

Precaution

Caution should be exercised when handling this chemical due to limited information on its health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 58920-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,2 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58920-75:
(7*5)+(6*8)+(5*9)+(4*2)+(3*0)+(2*7)+(1*5)=155
155 % 10 = 5
So 58920-75-5 is a valid CAS Registry Number.

58920-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-acetyl-1,3-dihydroinden-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2,2-diacetylindane

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:58920-75-5 SDS

58920-75-5Downstream Products

58920-75-5Relevant articles and documents

Mono- vs. dialkylation of carbanions. Effects of absolute and relative acidity of the conjugate carbon acids in selectivity control

Ridvan, Ludek,Zavada, Jiri

, p. 14793 - 14806 (2007/10/03)

The title problem was investigated in the reaction of the dibromide 1 with carbanions 2a-2g covering a range greater than 15 pK units in DMSO. It was found that the bis(monoalkylated) product 3 arises exclusively or predominantly from the carbanions 2d-2g derived from the less acidic carbon acids 7d-7g whereas the cyclic product of dialkylation 4 prevails in the reaction of the carbanions 2a-2c derived from the more acidic carbon acids 7a-7c. The alkylation selectivity thus depends critically on the absolute acidity of the carbon acid participating in the reaction. Rationale for this novel, and on basis of earlier studies unexpected finding is provided in terms of eqs. (1)-(4).

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