114853-35-9 Usage
Description
.beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)is a complex organic compound characterized by a beta-D-glucopyranoside sugar moiety and a 2-propenyl functional group attached to a 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene) group. .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-'s intricate structure, which includes both a sugar and an isoindole component, suggests that it may possess a range of biological activities or medicinal properties. This makes it a promising candidate for further research and development in the pharmaceutical and biotechnology industries.
Uses
Used in Pharmaceutical Industry:
.beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)is used as a potential therapeutic agent for various medical conditions due to its complex structure and the presence of biologically active moieties. .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-'s sugar component may facilitate interactions with cellular receptors, while the isoindole group could contribute to its pharmacological activity.
Used in Biotechnology Industry:
In the biotechnology sector, .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)may be utilized as a key component in the development of novel bioactive molecules or as a building block for creating new drugs with improved efficacy and selectivity. Its unique structure could be exploited to design molecules that target specific biological pathways or receptors, potentially leading to more effective treatments for various diseases.
Used in Drug Delivery Systems:
.beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-'s potential biological activities and complex structure make it a candidate for use in drug delivery systems. .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)could be employed as a carrier or targeting moiety for drug molecules, enhancing their delivery to specific cells or tissues and improving their overall therapeutic efficacy.
Used in Chemical Research:
As a complex organic compound with potentially interesting biological properties, .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)may also be used in chemical research to study the structure-activity relationships of similar compounds and to develop new synthetic methods for the preparation of related molecules with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 114853-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,5 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114853-35:
(8*1)+(7*1)+(6*4)+(5*8)+(4*5)+(3*3)+(2*3)+(1*5)=119
119 % 10 = 9
So 114853-35-9 is a valid CAS Registry Number.
114853-35-9Relevant articles and documents
Synthesis of the immunodominant trisaccharide related to the antigen from E. coli O126
Misra, Anup Kumar,Basu, Sumanta,Roy, Nirmolendu
, p. 2857 - 2862 (2007/10/03)
The trisaccharide derivative methyl 2-O-[4,6-di-O-acetyl-3-O-(2,3,4,6)-tetra-O-benzyl-α-D-gal-actopyranos yl)-2-deoxy-2-phthalimido-β-D-glucopyranosyl]-4,6-O-benzylidene-β-D- mannopyranoside (12) was obtained when 3-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopy
Chemical Synthesis of Nod-Rm-1: the Nodilation Factor Involved in Rhizobium meliloti-legume Symbiosis
Wang, Lai-Xi,Li, Chuan,Wang, Qin-Wei,Hui, Yong-Zheng
, p. 621 - 628 (2007/10/02)
A total synthesis of the sulfated lipotetrasaccharide (NodRm-1) is described.First, the disaccharide glycosyl donor - O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl chloride 3a or
Total synthesis of X hapten, III3 Fuc alpha-nLc4 Cer.
Sato,Ito,Nukada,Nakahara,Ogawa
, p. 197 - 210 (2007/10/02)
Total synthesis of O-beta-D-galactopyranosyl-(1----4)-O-[alpha-L- fucopyranosyl- (1----3)]-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-(1----3)-O-beta- D- galactopyranosyl- (1----4)-O-beta-D-glucopyranosyl-(1----1)-2-N-tetracosanoyl-(2S,3R ,4E)- sphinge
