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6318-49-6

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6318-49-6 Usage

Physical state

Colorless liquid

Odor

Sweet, fruity

Uses

Flavoring agent, fragrance ingredient in food and cosmetics industries

Synthesis

Precursor in the synthesis of various organic compounds

Health hazards

Potential irritant to skin, eyes, and respiratory system

Precautions

Safety measures should be taken when handling

Ingestion

May be hazardous if ingested

Storage and usage

Must be stored and used in accordance with proper safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 6318-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6318-49:
(6*6)+(5*3)+(4*1)+(3*8)+(2*4)+(1*9)=96
96 % 10 = 6
So 6318-49-6 is a valid CAS Registry Number.

6318-49-6Relevant articles and documents

ETHERS AND ESTERS OF 1-SUBSTITUTED CYCLOALKANOLS FOR USE AS AROMA CHEMICALS

-

, (2020/05/21)

The present invention relates to the use of an ether or an ester of a 1 -substituted cycloalkanol or of mixtures of two or more ethers or esters of 1 -substituted cycloalkanols or of a stereoisomer thereof or of a mixture of two or more stereoisomers thereof as aroma chemicals; to the use thereof for modifying the scent character of a fragranced composition; to an aroma chemical composition containing an ether or an ester of a 1 -substituted cycloalkanol or of mixtures of two or more ethers or esters of 1 -substituted cycloalkanols or of a stereoisomer thereof or of a mixture of two or more stereoisomers thereof; and to a method of preparing a fragranced composition or for modifying the scent character of a fragranced composition. The invention further relates to specific ethers or esters of 1 -substituted cycloalkanols.

Practical synthesis of allylic silanes from allylic esters and carbamates by stereoselective copper-catalyzed allylic substitution reactions

Oestreich, Martin,Auer, Gertrud

, p. 637 - 640 (2007/10/03)

The first copper-catalyzed allylic substitution reactions of allylic acetates and carbamates employing a bis(triorganosilyl)zinc reagent are reported. This novel procedure avoids the use of stoichiometric amounts of copper salts which are usually mandatory with this chemistry. Application of this methodology to standard model substrates substantiates a high diastereoselectivity for the double bond geometry (E:Z) as well as the relative configuration (syn:anti).

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