Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

167904-07-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 167904-07-6 Structure
  • Basic information

    1. Product Name: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone
    2. Synonyms: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone
    3. CAS NO:167904-07-6
    4. Molecular Formula:
    5. Molecular Weight: 538.64
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 167904-07-6.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: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone(167904-07-6)
    11. EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone(167904-07-6)
  • 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: 167904-07-6(Hazardous Substances Data)

167904-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167904-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,9,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167904-07:
(8*1)+(7*6)+(6*7)+(5*9)+(4*0)+(3*4)+(2*0)+(1*7)=156
156 % 10 = 6
So 167904-07-6 is a valid CAS Registry Number.

167904-07-6Downstream Products

167904-07-6Relevant articles and documents

Direct one-pot highly enantioselective assembly of polyketide and carbohydrate synthons

Zhao, Gui-Ling,Liao, Wei-Wei,Córdova, Armando

, p. 4929 - 4932 (2007/10/03)

A short, direct, catalytic, enantioselective synthesis of polyketide segments and carbohydrates is presented. The novel, direct, one-pot, organocatalytic asymmetric tandem cross-aldol/Horner-Wittig-Emmons reactions assemble polyketide and carbohydrate der

A Novel and Practical Synthesis of L-Hexoses from D-Glycono-1,5-lactones

Takahashi, Hideyo,Hitomi, Yuko,Iwai, Yoshinori,Ikegami, Shiro

, p. 2995 - 3000 (2007/10/03)

A novel and efficient conversion of D-glycono-1,5-lactones into the corresponding L-sugars is described. The important intermediate, δ-hydroxyalkoxamates, was provided by a practical alkoxyamination of D-glycono-1,5-lactones mediated by Me3Al.

Intramolecular Tishchenko reactions of protected hexos-5-uloses: A novel and efficient synthesis of L-idose and L-altrose

Adinolfi,Barone,De Lorenzo,Iadonisi

, p. 336 - 338 (2007/10/03)

Protected t-butyl esters of aldonic acids with the rare L-ido and L- altro configuration can be effectively obtained by a diastereoselective Tishchenko reaction of hexos-5-uloses induced by t-BuOSmI2. These compounds can be easily converted int

40. Synthesis of galactose- and N-acetylglucosamine-derived tetrazoles and their evaluation as β-glycosidase inhibitors

Heightman,Ermert,Klein,Vasella

, p. 514 - 532 (2007/10/02)

The title compounds 6 and 7 have been prepared from the known 2,3-di-O-benzyl-4,6-O-benzylidene-D-galactose (18) and N2-acetyl-tri-O-benzyl-D-glucosamine oxime (29) in eight and six steps, respectively. The azidonitrile leading to the benzylate

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 167904-07-6