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956317-01-4

3,6-anhydro-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 956317-01-4 Structure

  • Basic information

    1. Product Name: 3,6-anhydro-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone
    2. Synonyms: 3,6-anhydro-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone
    3. CAS NO:956317-01-4
    4. Molecular Formula:
    5. Molecular Weight: 340.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 956317-01-4.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: 3,6-anhydro-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,6-anhydro-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone(956317-01-4)
    11. EPA Substance Registry System: 3,6-anhydro-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone(956317-01-4)

  • 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: 956317-01-4(Hazardous Substances Data)

956317-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956317-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,3,1 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 956317-01:
(8*9)+(7*5)+(6*6)+(5*3)+(4*1)+(3*7)+(2*0)+(1*1)=184
184 % 10 = 4
So 956317-01-4 is a valid CAS Registry Number.

956317-01-4Relevant articles and documents

Enantiodivergent synthesis of cytotoxic styryl lactones from d-xylose. The first total synthesis of (+)- and (-)-crassalactone C

Popsavin, Velimir,Benedekovi?, Goran,Sre?o, Bojana,Francuz, Jovana,Popsavin, Mirjana,Koji?, Vesna,Bogdanovi?, Gordana,Divjakovi?, Vladimir

experimental part, p. 10596 - 10607 (2010/03/03)

Enantiodivergent total syntheses of both (+)- and (-)-enantiomers of goniofufurone, 7-epi-goniofufurone and crassalactone C have been accomplished starting from d-xylose. The key steps of the synthesis of 7-epi-(+)-goniofufurone were a stereo-selective ad

Divergent synthesis of cytotoxic styryl lactones from D-xylose. The first total synthesis of (+)-crassalactone C

Popsavin, Velimir,Benedekovic, Goran,Sreco, Bojana,Popsavin, Mirjana,Francuz, Jovana,Kojic, Vesna,Bogdanovic, Gordana

, p. 4235 - 4238 (2008/02/12)

A new divergent approach to (+)-goniofufurone (1) and 7-epi-(+)- goniofufurone (2), as well as the first total synthesis of crassalactone C (3), has been achieved starting from o-xylose. In a preliminary bioassay, all three natural products 1, 2, and 3 sh

Stereospecific α-alkoxystannane couplings with acyl chlorides: Total synthesis of (+)-goniofufurone

Ye, Jianhua,Bhatt, Rama K.,Falck

, p. 8007 - 8010 (2007/10/02)

Stereospecific C-glycoside formation via Pd/Cu mediated coupling of PhCOCl with cyclic α-alkoxystannane 6, derived from D-glucurono-6,3-lactone, was the key transformation in a concise total synthesis of the anticancer agent (+)-goniofufurone.

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