61434-50-2 Usage
Description
(1E)-3,7-dimethylocta-1,6-diene-1,3-diol, a diol with the molecular formula C10H18O2, is a colorless liquid at room temperature. It features two hydroxyl (OH) groups and a double bond in its structure, which allows for versatile chemical reactions. The presence of methyl branches enhances its stability and reactivity in organic synthesis.
Uses
Used in Organic Synthesis:
(1E)-3,7-dimethylocta-1,6-diene-1,3-diol is used as a versatile building block for the synthesis of various organic compounds due to its double bond and reactivity.
Used in Fragrance Industry:
(1E)-3,7-dimethylocta-1,6-diene-1,3-diol is used as a key intermediate in the production of fragrances, contributing to the creation of unique scents.
Used in Pharmaceutical Industry:
(1E)-3,7-dimethylocta-1,6-diene-1,3-diol is used as a starting material for the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 61434-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,3 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61434-50:
(7*6)+(6*1)+(5*4)+(4*3)+(3*4)+(2*5)+(1*0)=102
102 % 10 = 2
So 61434-50-2 is a valid CAS Registry Number.
61434-50-2Relevant articles and documents
Biotransformation of linalool to furanoid and pyranoid linalool oxides by Aspergillus niger
Demyttenaere, Jan C.R.,Willemen, Hendra M.
, p. 1029 - 1036 (2007/10/03)
Biotransformation of (±)-linalool with submerged shaking cultures of Aspergillus niger, particularly A. niger ATCC 9142, yielded a mixture of cis- and trans-furanoid linalool oxide (yield 15-24%) and cis- and trans-pyranoid linalool oxide (yield 5-9%). Biotransformation of (R)-(-)-linalool with the same strain yielded almost pure trans-furanoid and trans-pyranoid linalool oxide (ee > 95). These conversions were purely biocatalytic, since in acidified water (pH 3.5) almost 50% linalool was recovered unchanged, the rest was lost by evaporation. The biotransformation was also carried out with growing surface cultures.
Alkylation du linalol sur les carbones C8 (et C6)
Cuvigny, Therese,Julia, Marc,Rolando, Christian
, p. 9 - 28 (2007/10/02)
Metallation of linalool α to the distal double bond with strong bases is described.The corresponding carbanions have been alkylated or oxidized to give mixtures of products resulting from attack at both carbon 8 (major product) and carbon 6 (minor product).