1621066-64-5 Usage
Description
(1S)-2,2',3,3'-tetrahydro-6,6'-dimethyl-1,1'-Spirobi[1H-indene]-7,7'-diol, also known as (1S,2S,7S)-diol, is a synthetic chemical compound with a spirobiindane structure. It is a chiral molecule with two chiral centers, and the (1S,2S,7S) configuration refers to the stereochemistry of the hydroxyl groups at positions 1, 2, and 7.
Uses
Used in Organic Synthesis:
(1S)-2,2',3,3'-tetrahydro-6,6'-dimethyl-1,1'-Spirobi[1H-indene]-7,7'-diol is used as a chiral building block for the production of various types of drugs and bioactive molecules. Its unique spirobiindane structure and chiral nature make it a valuable reagent for creating complex chemical structures with high stereochemical control.
Used in Pharmaceutical Research:
(1S)-2,2',3,3'-tetrahydro-6,6'-dimethyl-1,1'-Spirobi[1H-indene]-7,7'-diol is used as a chiral building block in the development of new medicines and pharmaceuticals. Its unique spirobiindane structure and chiral nature make it a valuable tool for creating complex chemical structures with high stereochemical control, which is essential for the development of effective and selective drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 1621066-64-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,1,0,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1621066-64:
(9*1)+(8*6)+(7*2)+(6*1)+(5*0)+(4*6)+(3*6)+(2*6)+(1*4)=135
135 % 10 = 5
So 1621066-64-5 is a valid CAS Registry Number.
1621066-64-5Relevant articles and documents
Asymmetric reductive coupling of dienes and aldehydes catalyzed by nickel complexes of spiro phosphoramidites: Highly enantioselective synthesis of chiral bishomoallylic alcohols
Yang, Yun,Zhu, Shou-Fei,Duan, Hai-Feng,Zhou, Chang-Yue,Wang, Li-Xin,Zhou, Qi-Lin
, p. 2248 - 2249 (2007/10/03)
A highly efficient nickel-catalyzed asymmetric reductive coupling of dienes and aldehydes has been realized by using bulky spirobiindane phosphoramidite ligands, affording bishomoallylic alcohols in high yields with excellent diastereoselectivities and en
