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methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72904-78-0 Structure
  • Basic information

    1. Product Name: methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside
    2. Synonyms: methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside
    3. CAS NO:72904-78-0
    4. Molecular Formula:
    5. Molecular Weight: 266.294
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72904-78-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside(72904-78-0)
    11. EPA Substance Registry System: methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside(72904-78-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 72904-78-0(Hazardous Substances Data)

72904-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72904-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72904-78:
(7*7)+(6*2)+(5*9)+(4*0)+(3*4)+(2*7)+(1*8)=140
140 % 10 = 0
So 72904-78-0 is a valid CAS Registry Number.

72904-78-0Relevant articles and documents

The 2α-(3-hydroxypropyl) group as an active motif in vitamin D3 analogues as agonists of the mutant vitamin D receptor (Arg274Leu)

Honzawa, Shinobu,Yamamoto, Yasuhiro,Yamashita, Atsushi,Sugiura, Takayuki,Kurihara, Masaaki,Arai, Midori A.,Kato, Shigeaki,Kittaka, Atsushi

, p. 3002 - 3024 (2008/09/20)

We designed and synthesized 1α- and 1β-hydroxymethyl-2α-(3-hydroxypropyl)-25-hydroxyvitamin D3 (2a,b) and related analogues 2α-(3-hydroxypropyl)-25-hydroxyvitamin D3 (3), Posner's analogues of 1α- and 1β-hydroxymethyl-25-hydroxyvitamin D3 (4a,b), as well as 2α-(3-hydroxypropyl)-1α,25-dihydroxyvitamin D3 (5), to confirm the effect of the 1α-hydroxy group and/or 2α-(3-hydroxypropyl) group of vitamin D3 analogues with the modified A-ring moiety on the mutant vitamin D receptor, VDR(Arg274Leu). The 2α-(3-hydroxypropyl) group showed better effect on enhancement of the transcriptional activity through the mutant VDR than the 1α- and 1β-hydroxymethyl groups.

Total synthesis of calystegine A7

Csuk, René,Prell, Erik,Rei?mann, Stefan

, p. 9417 - 9422 (2008/12/22)

A straightforward chiral pool synthesis for the glycosidase inhibitor calystegine A7 (isolated from Lycium chinense) from methyl α-d-glucopyranoside is described. Keysteps of this synthesis include a ultrasound assisted Zn-mediated tandem ring

Synthesis of 24,24-ethanovitamin D3 lactones using ruthenium-catalyzed intermolecular enyne metathesis: Potent vitamin D receptor antagonists

Saito, Nozomi,Masuda, Manami,Saito, Hiroshi,Takenouchi, Kazuya,Ishizuka, Seiichi,Namekawa, Jun-Ichi,Takimoto-Kamimura, Midori,Kittaka, Atsushi

, p. 2533 - 2543 (2007/10/03)

Novel vitamin D receptor antagonists, 24,24-ethanovitamin D 3-26,23-lactones 6 and 7 and their 2α-functionalized analogues 6a-c and 7a-c were synthesized and their biological activities were evaluated. The triene structure of vitamin D3/s

Enantioselective synthesis of phyllanthurinolactone, a leaf-closing substance of Phyllanthus urinaria L., and its analogs toward the development of molecular probes

Urakawa, Yoshifumi,Sugimoto, Takanori,Sato, Hirotaka,Ueda, Minoru

, p. 5885 - 5888 (2007/10/03)

We report enantioselective synthesis of phyllanthurinolactone (1), a leaf-closing substance of Phyllanthus urinaria L., and its analogs with sugars other than D-glucose. Structure-activity relationship study using them revealed that the structure of the sugar moiety did not affect their bioactivity at all. This result is very important for the development of molecular probes based on the structure of 1.

Enantiomerically pure decalinic structures from carbohydrates using intramolecular Diels-Alder and Ferrier carbocyclization

Taillefumier, Claude,Chapleur, Yves

, p. 708 - 722 (2007/10/03)

The synthesis of enantiomerically pure decalinic structures, advanced intermediates for the synthesis of the hexahvdronaphtalen part of mevinic acids, is described. The key steps are the intramolecular Diels-Alder cycloaddition of a suitably substituted sugar enone obtained via the Ferrier rearrangement of tri-O-acetyl-D-glucal with the appropriate alcohol representing the diene part of the system. Chemical manipulation of the resulting. diastereomerically pure, cycloadduct led to a 5,6-unsaturated carbohydrate which was submitted to the Ferrier carbocylization. This reaction proved difficult likely because of the embedding of the aglycon in a cycle, the hydration product of the double bond being the main product. This compound was in turn transformed into the decalinic structures by treatment in basic medium. The inverse strategy. Ferrier carbocyclization followed by IMDA of an enone and a diene linked via an ester bond was unsuccessful.

The Deoxygenation of Some Carbohydrate Diols via Derived Cyclic Thiocarbonate

Patroni, Joseph J.,Stick, Robert V.,Engelhardt, Lutz M.,White, Allan H.

, p. 699 - 711 (2007/10/02)

The treatment of methyl 2,6-di-O-methyl-3,4-O-thiocarbonyl-β-D-galactoside with methyl iodide gives mainly the 3-deoxy-3-iodo-D-guloside, whereas the α-anomer of the above and methyl 2-O-methyl-3,4-O-thiocarbonyl-β-L-arabinoside give mainly the 4-deoxy-4-

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