Welcome to LookChem.com Sign In|Join Free

CAS

  • or

147237-44-3

N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147237-44-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

  • N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea

    Cas No: 147237-44-3

  • Need to discuss

  • No requirement

  • Adequate

  • COLORCOM LTD.
  • Contact Supplier

  • N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea

    Cas No: 147237-44-3

  • Need to discuss

  • No requirement

  • Adequate

  • Xinyang Longye Chemical CO.,LTD
  • Contact Supplier
  • 147237-44-3 Structure

  • Basic information

    1. Product Name: N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea
    2. Synonyms: N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea
    3. CAS NO:147237-44-3
    4. Molecular Formula:
    5. Molecular Weight: 760.906
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147237-44-3.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: N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea(CAS DataBase Reference)
    10. NIST Chemistry Reference: N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea(147237-44-3)
    11. EPA Substance Registry System: N'-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-N-<<1R-(1α,2β,3α,4β,5β)>-1-(hydroxymethyl)-1,2,3,4-tetrahydroxycyclopent-5-yl>thiourea(147237-44-3)

  • 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: 147237-44-3(Hazardous Substances Data)

147237-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147237-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,3 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147237-44:
(8*1)+(7*4)+(6*7)+(5*2)+(4*3)+(3*7)+(2*4)+(1*4)=133
133 % 10 = 3
So 147237-44-3 is a valid CAS Registry Number.

147237-44-3Relevant articles and documents

Total Synthesis of the Trehalase Inhibitors Trehalostatin and Trehazolin, and of Their Diastereoisomers. Final Structural Confirmation of the Inhibitor

Uchida, Chikara,Yamagishi, Tatsuya,Ogawa, Seiichiro

, p. 589 - 602 (2007/10/02)

Potent trehalase inhibitors 1-4 have been synthesized, thereby establishing both the structure and the absolute configuration of the known inhibitor trehazolin 2.Compound 1, previously proposed as the structure of trehalostatin, and its diastereoisomer 3,

Syntheses of trehazolin, trehalamine, and the aminocyclitol moiety of trehazolin: Determination of absolute configuration of trehazolin

Kobayashi,Miyazaki,Shiozaki

, p. 813 - 822 (2007/10/02)

The syntheses and determination of the absolute configuration of trehazolin (1), its aglycon (trehalamine (3), and its aminocyclitol hexaacetate moiety (5) are described. An important intermediate, optically active epoxide 16α, was obtained from an 11-ste

Total Synthesis of Trehalase Inhibitor, Trehazolin

Ogawa, Seiichiro,Uchida, Chikara

, p. 173 - 176 (2007/10/02)

The total synthesis of trehalase inhibitor, trehazolin has been accomplished by coupling the optically active aminocyclopentanepentaol with α-D-glucopyranosylisothiocyanate derivative, followed by subsequent oxazoline-ring formation and removal of the pro

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 147237-44-3