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3-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85315-67-9 Structure
  • Basic information

    1. Product Name: 3-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose
    2. Synonyms: 3-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose
    3. CAS NO:85315-67-9
    4. Molecular Formula:
    5. Molecular Weight: 364.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85315-67-9.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-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose(85315-67-9)
    11. EPA Substance Registry System: 3-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose(85315-67-9)
  • 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: 85315-67-9(Hazardous Substances Data)

85315-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85315-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,1 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85315-67:
(7*8)+(6*5)+(5*3)+(4*1)+(3*5)+(2*6)+(1*7)=139
139 % 10 = 9
So 85315-67-9 is a valid CAS Registry Number.

85315-67-9Downstream Products

85315-67-9Relevant articles and documents

Synthesis and biological evaluation of thymine nucleosides fused with 3′,4′-tetrahydrofuran ring

Kim, Myong Jung,Kim, Hea Ok,Kim, Hee-Doo,Kim, Joong Hyup,Jeong, Lak Shin,Chun, Moon Woo

, p. 3499 - 3501 (2003)

The pyrimidine nucleosides fused with 3′,4′-tetrahydrofuran ring were successfully synthesized, starting from 1,2; 5,6-di-O-isopropylidene-D-glucose and assayed for antiviral activities against HIV-1, HIV-2, EMCV, Cox. B3 and VSV. Thymine analogue (5) and

Synthesis and biological evaluation of pyrimidine nucleosides fused with 3′,4′-tetrahydrofuran ring

Chun, Moon Woo,Kim, Myong Jung,Kim, Hea Ok,Moon, Hyung Ryong,Kim, Hee-Doo,Kim, Joong Hyup,Jeong, Lak Shin

, p. 719 - 721 (2007/10/03)

Pyrimidine nucleosides fused with 3′,4′-tetrahydrofuran ring were synthesized, starting from 1,2;5,6-di-O-isopropylidene-D-glucose and assayed for antiviral activities. Thymine analogue 1 and its corresponding 2′-deoxy analogue 3 exhibited high cytotoxici

Synthesis of novel 3′-deoxy-3′-C-hydroxymethyl nucleosides with conformationally rigid sugar moiety as potential antiviral agents

Moon Woo Chun,Myung Jung Kim,Un Hee Jo,Joong Hyup Kim,Kim,Lak Shin Jeong

, p. 699 - 702 (2007/10/03)

Based on the fact that the ring expanded 3′-C-hydroxymethyl analogue of oxetanocin A exhibited potent antiviral activity, two types of conformationally rigid 3′-C-hydroxymethyl derivatives in which 2′-hydroxyl group is linked to the 4′-position or to the 6′-position were synthesized starting from 1,2;5,6-di-O-isopropylidene-D-glucose, respectively.

Synthesis of a phosphinic acid analogue of cyclic AMP

Regan,Sciammetta,Tattersall

, p. 8211 - 8215 (2007/10/03)

Synthesis of a cyclic phosphinate ester analogue of cyclic AMP was achieved by using a double Arbuzov-type cyclisation of bis-trimethylsilyl phosphonite onto a sugar dihalide derivative as the key step. (C) 2000 Elsevier Science Ltd.

Chiral Synthesis of Polyketide-derived Natural Products. Part 5. Synthesis of a Chiral Segment Corresponding to the C-1-C-5 Unit of Erythromycin A from D-Glucose

Oikawa, Yuji,Nishi,Takao,Yonemitsu, Osamu

, p. 19 - 26 (2007/10/02)

As a right-hand segment with three consecutive chiral centres corresponding to the C-1-C-5 unit of erythromycin A (1), (2S,3R,4S)-3,5-isopropylidenedioxy-2,4-dimethylpentanal (32) was synthesized from D-glucose (5) by application of MPM (4-methoxybenzyl)

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