99328-46-8 Usage
Uses
Used in Perfumery and Cosmetics Industry:
5-Methyl-1-hepten-4-ol is used as a fragrance ingredient for its pleasant rose-like scent, enhancing the aroma of perfumes and cosmetic products.
Used in Household Cleaning Products and Air Fresheners Industry:
5-Methyl-1-hepten-4-ol is used as an air freshening agent for its floral scent, providing a pleasant atmosphere in homes and other indoor spaces.
Used in Pharmaceutical Applications:
5-Methyl-1-hepten-4-ol is used as an antimicrobial agent for its ability to inhibit the growth of certain microorganisms, contributing to the development of pharmaceutical products with antibacterial properties.
Used in Flavor Industry:
5-Methyl-1-hepten-4-ol is used as a flavoring agent for its unique and pleasant aroma, adding a floral note to various food and beverage products.
Check Digit Verification of cas no
The CAS Registry Mumber 99328-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,2 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99328-46:
(7*9)+(6*9)+(5*3)+(4*2)+(3*8)+(2*4)+(1*6)=178
178 % 10 = 8
So 99328-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-4-6-8(9)7(3)5-2/h4,7-9H,1,5-6H2,2-3H3
99328-46-8Relevant academic research and scientific papers
Chiral Synthesis via Organoboranes. 21. Allyl- and Crotylboration of α-Chiral Aldehydes with Diisopinocampheylboron as the Chiral Auxiliary
Brown, Herbert C.,Bhat, Krishna S.,Randad, Ramnarayan S.
, p. 1570 - 1576 (2007/10/02)
B-Allyldiisopinocampheylboranes have been screened for diastereofacial selectivity in their reaction with α-substituted chiral aldehydes.Both syn and anti products have been obtained in very high diastereoselectivities.Further, (E)-crotyldiisopinocampheylboranes and (Z)-crotyldiisopinocampheylboranes have been used for diastereofacial selectivity in their reaction with α-substituted chiral aldehydes.These crotylboranes, 20-23, are highly diastereoselective reagents and the corresponding (3,4- and 4,5-)-anti,syn, -anti,anti, and -syn,anti products have been obtained in very high facial selectivities; even the syn,syn product has been obtained in moderately good facial selectivity.Finally, the relative efficiences of the various chiral auxiliaries utilized in the literature for the allyl- and crotylboration have been compared with those achieved by the diisopinocampheylboron moiety.
