123001-17-2 Usage
Chemical structure
A glycerol backbone with two long carbon chains (tetradecyl groups) attached at the first and second positions, and two glucose molecules attached in a complex configuration at the third position.
Classification
Belongs to the class of glycolipids, which are important components of biological membranes.
Occurrence
Often found in nature.
Biological and pharmacological activities
Studied for its potential role in cell signaling and as a therapeutic agent for various diseases.
Applications
Potential applications in the fields of biochemistry and medicine due to its complex structure and interesting properties.
Check Digit Verification of cas no
The CAS Registry Mumber 123001-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,0 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123001-17:
(8*1)+(7*2)+(6*3)+(5*0)+(4*0)+(3*1)+(2*1)+(1*7)=52
52 % 10 = 2
So 123001-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C43H84O13/c1-4-7-9-11-13-15-17-19-21-23-25-27-30-53-42(49)39(48)35(33-52-40-38(47)37(46)36(45)34(32-44)55-40)56-41(51-29-6-3)43(42,50)54-31-28-26-24-22-20-18-16-14-12-10-8-5-2/h34-41,44-50H,4-33H2,1-3H3/t34-,35-,36-,37+,38-,39-,40-,41-,42-,43-/m1/s1
123001-17-2Relevant articles and documents
Synthesis of Glycoglycerolipids: 3-O-Mannooligosyl-1,2-di-O-tetradecyl-sn-glycerol
Ogawa, Tomoya,Beppu, Kazuo
, p. 263 - 268 (2007/10/02)
Synthetic routes for the following mannooligosylglycerolipids of biological interest were developed by using regioselectively protected monosaccharide synthons and 1,2-di-O-alkyl-sn-glycerol; 3-O-(2-O-α-D-mannopyranosyl-α-D-mannopyranosyl)-1,2-di-O-tetrad
