99328-46-8 Usage
General Description
5-Methyl-1-hepten-4-ol, also known as rose oxide, is a colorless liquid with a floral, rose-like odor. It is a naturally occurring fragrance compound found in various flowers such as roses, jasmine, and lilies. This chemical is commonly used in perfumery and cosmetic products due to its pleasant scent. It is also a valuable ingredient in household cleaning products and air fresheners. Additionally, 5-methyl-1-hepten-4-ol is known for its antimicrobial properties and is used in some pharmaceutical applications. Overall, this chemical plays a significant role in the fragrance and flavor industry due to its unique and pleasant aroma.
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 articles and documents
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.
