848827-37-2 Usage
Chemical structure
1,3-Dioxolane ring with an azide group, a chiral center, and a pentyl group.
Chirality
The compound has a chiral center denoted by the (1S) designation, indicating its stereochemistry.
Isomer
The compound is classified as a 4S,5R isomer.
Functional groups
The compound contains an azide functional group and a pentyl group.
Potential applications
The compound has potential applications in various fields, including pharmaceuticals, research, and industrial processes.
Safety precautions
Due to its intricate structure and azide functional group, proper handling and safety precautions are essential when working with 1,3-Dioxolane,
4-[(1S)-1-azido-2-(triphenylmethoxy)ethyl]-2,2-dimethyl-5-pentyl-,
(4S,5R)-.
Check Digit Verification of cas no
The CAS Registry Mumber 848827-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,8,2 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 848827-37:
(8*8)+(7*4)+(6*8)+(5*8)+(4*2)+(3*7)+(2*3)+(1*7)=222
222 % 10 = 2
So 848827-37-2 is a valid CAS Registry Number.
848827-37-2Relevant academic research and scientific papers
Synthesis of α-galactosyl ceramide and the related glycolipids for evaluation of their activities on mouse splenocytes
Fan, Gang-Ting,Pan, Yi-Shin,Lu, Kuo-Cheng,Cheng, Yu-Pei,Lin, Wan-Chen,Lin, Steven,Lin, Chun-Hung,Wong, Chi-Huey,Fang, Jim-Min,Lin, Chun-Cheng
, p. 1855 - 1862 (2007/10/03)
Phytosphingosine and its short-chain analog were efficiently synthesized with 19% overall yield in 10 steps, respectively, starting from an inexpensive d-lyxose. Galactosyl donors of sulfide and phosphite types bearing benzoyl protecting groups of 4- and
