129705-30-2 Usage
General Description
"(3S,6S)-2,7-DIMETHYL-3,6-OCTANEDIOL" is a chemical compound with the molecular formula C10H22O2. It is an organic compound that belongs to the family of alcohols. (3S,6S)-2,7-DIMETHYL-3,6-OCTANEDIOL is classified as a diol, meaning it contains two hydroxyl groups. It has a specific stereochemistry, with a configuration of (3S,6S), which refers to the arrangement of the substituent groups around the chiral centers. (3S,6S)-2,7-DIMETHYL-3,6-OCTANEDIOL is often used as a building block in the synthesis of complex organic molecules, and its hydroxyl groups make it a versatile intermediate for the preparation of various derivatives with different properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 129705-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,0 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129705-30:
(8*1)+(7*2)+(6*9)+(5*7)+(4*0)+(3*5)+(2*3)+(1*0)=132
132 % 10 = 2
So 129705-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O2/c1-7(2)9(11)5-6-10(12)8(3)4/h7-12H,5-6H2,1-4H3/t9-,10-/m0/s1
129705-30-2Relevant articles and documents
Synthesis of (±)-trans-2,5-diisopropylborolane
Laschober, Gerhard,Zorzi, Massimo,Hodgetts, Kevin J.
, p. 244 - 252 (2001)
The cyclic hydroboration of 2,7-dimethyl-2,6-octadiene (6) was studied. It was found that the stereochemical outcome of the reaction was dependent upon the solvent, temperature, time and the nature of the borane reagent. Pure racemic trans-2,5-diisopropyl
Remote Stereocontrol by utilizing Intramolecular Carbonyl Reduction with Boranes
Harada, Toshiro,Matsuda, Yasuhiro,Imanaka, Satoru,Oku, Akira
, p. 1641 - 1643 (2007/10/02)
A simple and efficient method for the remote (1,4- and/or 1,5-) stereocontrol was realized by utilizing an intramolecular carbonyl reduction with ThexBH2 (Thex = 1,1,2-trimethylpropyl).
