943307-50-4 Usage
General Description
Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is a complex chemical compound with a molecular structure that includes benzyl, chloroacetyl, and rhamnopyranoside moieties. The allyl group serves as a linker between these components. Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is a glycoside, a type of sugar derivative, and it is commonly used in organic synthesis and medicinal chemistry. It has potential applications in the development of new pharmaceuticals and bioactive compounds due to its unique chemical properties. Overall, Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is a versatile chemical with diverse potential uses in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 943307-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,3,0 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 943307-50:
(8*9)+(7*4)+(6*3)+(5*3)+(4*0)+(3*7)+(2*5)+(1*0)=164
164 % 10 = 4
So 943307-50-4 is a valid CAS Registry Number.
943307-50-4Relevant articles and documents
Silver(I) oxide-mediated regioselective 2-monoacylation in 3-O-benzyl-α-l-rhamnopyranosides and application in synthesis of a protected tetrasaccharide fragment of potent cytotoxic saponins gleditsiosides C and D
Yang, Qian,Lei, Ming,Yin, Qin-Jian,Yang, Jin-Song
, p. 1175 - 1181 (2008/02/02)
The axial 2-hydroxyl group of methyl and allyl 3-O-benzyl-α-l-rhamnopyranosides was selectively acylated in 56-78% yields by reaction with 1.1 equiv of acyl chloride in the presence of 1.5 equiv of silver(I) oxide. Use of the method permitted a convenient
