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10292-98-5

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10292-98-5 Usage

General Description

Epicamphor is a chemical compound that is derived from camphor, a natural substance found in several plants. It is used primarily as a flavoring agent in the food and beverage industry, providing a cooling and refreshing sensation. Epicamphor is also utilized in the production of fragrances and cosmetics due to its pleasant aroma and invigorating properties. Additionally, it has potential applications in the pharmaceutical and medical industries for its anti-inflammatory and analgesic properties. However,

Check Digit Verification of cas no

The CAS Registry Mumber 10292-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10292-98:
(7*1)+(6*0)+(5*2)+(4*9)+(3*2)+(2*9)+(1*8)=85
85 % 10 = 5
So 10292-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-9(2)7-4-5-10(9,3)6-8(7)11/h7H,4-6H2,1-3H3/t7-,10+/m0/s1

10292-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-epicamphor

1.2 Other means of identification

Product number -
Other names epicamphre-(-)

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:10292-98-5 SDS

10292-98-5Relevant articles and documents

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Rupe,Martin

, p. 1207,1212 (1934)

-

MERCURATION OF BORNYLENE. EFFECT OF THE ELECTROPHILICITY OF THE REAGENT AND SOLVENT ON THE RATIO OF REACTION PRODUCTS

Skorobogatova, E. V.,Povelikina, L. N.,Kartashov, V. N.

, p. 1979 - 1982 (2007/10/02)

In the mercuration of bornylene a Wagner-Meerwein rearrangement takes place in addition to the path leading to the formation of exo-addition products.The ratio between the reaction products varies over a wide range, depending on nature of the reagent and the solvent.It is suggested that the structure of the intermediate acquires the character of an unsymmetrical β-mercury-containig ion with increase in the hardness of the electrophilic reagent.

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