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24348-06-9

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24348-06-9 Usage

Description

[1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is a bicyclic ketone chemical compound characterized by its complex molecular structure, featuring a hydroxyl group and three methyl substituents. [1R-(1alpha,4beta,6alpha)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is known for its rigid and compact structure due to the presence of the bicyclo[4.1.0]heptane framework.

Uses

Used in Fragrance Industry:
[1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is used as a fragrance ingredient for its pleasant, woody odor. It is commonly utilized in the production of perfumes, colognes, and other scented products, contributing to their overall aroma.
Used in Flavor Industry:
In the flavor industry, [1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is used as a flavoring agent. It is added to various food and beverage products to enhance their aroma and taste, providing a unique and desirable sensory experience for consumers.
Used in Cosmetic Industry:
[1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is also employed in the cosmetic industry, where it serves as a key ingredient in the formulation of scented products such as lotions, creams, and other personal care items. Its woody odor adds a pleasant and appealing fragrance to these products, making them more attractive to consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 24348-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,4 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24348-06:
(7*2)+(6*4)+(5*3)+(4*4)+(3*8)+(2*0)+(1*6)=99
99 % 10 = 9
So 24348-06-9 is a valid CAS Registry Number.

24348-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one

1.2 Other means of identification

Product number -
Other names 3|A-Hydroxyandrosta-5,15-dien-17-one

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:24348-06-9 SDS

24348-06-9Downstream Products

24348-06-9Relevant articles and documents

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Carson,M.S. et al.

, p. 2220 - 2223 (1969)

-

SYNTHESIS OF METHYL 1R-CIS-2,2-DIMETHYL-3-(2-OXOPROPYL)CYCLOPROPANECARBOXYLATE, AN INTERMEDIATE FOR SYNTHETIC PYRETHROIDS

Muljiani, Z.,Deshmukh, A. R. A. S.,Gadre, S. R.,Joshi, V. S.

, p. 25 - 32 (2007/10/02)

Synthesis of keto ester (1) from (+)-3-carene is described.Ring cleavage is effected by the Beckmann Fragmentation.

Chromic Acid Oxidation of Some Oxiranes

Krishna, R. R.,Chawla, H. P. S.,Dev, Sukh

, p. 1190 - 1196 (2007/10/02)

Oxiranes derived from some alkenes, with olefinic bonds present in different stereoelectronic environments, have been treated with Cr(VI)-reagents.The major products obtained have been identified and their formation rationalized.In some cases, the method becomes synthetically useful for C-C bond cleavage.

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