Welcome to LookChem.com Sign In|Join Free

CAS

  • or

62414-75-9

2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is a chemical compound derived from alpha-D-arabinopyranose and isothiocyanate, featuring three acetyl groups attached to the sugar backbone. It possesses potential biological and pharmacological applications, particularly in the areas of anticancer and antifungal properties. As a promising drug candidate, it is under research for its potential in the development of new pharmaceuticals and bioactive compounds. Further studies are required to fully explore its potential benefits and applications.

62414-75-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 62414-75-9 Structure

  • Basic information

    1. Product Name: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE
    2. Synonyms: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE;AITC;2,3,4-tri-o-acetyl-α-d-arabinopyranosyl isothiocyanate;2,3,4-tri-O-acetylarabinopyranosyl isothiocyanate
    3. CAS NO:62414-75-9
    4. Molecular Formula: C12H15NO7S
    5. Molecular Weight: 317.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62414-75-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 401.6°C at 760 mmHg
    3. Flash Point: 196.7°C
    4. Appearance: /
    5. Density: 1.4g/cm3
    6. Vapor Pressure: 1.17E-06mmHg at 25°C
    7. Refractive Index: 1.561
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. BRN: 1690031
    11. CAS DataBase Reference: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE(62414-75-9)
    13. EPA Substance Registry System: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE(62414-75-9)

  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 36/37/38-42
    3. Safety Statements: 23-26-36
    4. WGK Germany: 3
    5. RTECS:
    6. F: 9
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 62414-75-9(Hazardous Substances Data)

62414-75-9 Usage

Uses

Used in Pharmaceutical Industry:
2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is used as a potential drug candidate for its anticancer properties. It has been the subject of research for its ability to target and inhibit the growth of cancer cells, making it a promising agent in the fight against various types of cancer.
Used in Antifungal Applications:
In the field of antifungal research, 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is utilized for its potential to combat fungal infections. Its antifungal properties are being studied to develop new treatments for various fungal diseases.
Used in Bioactive Compound Development:
2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is employed in the development of new bioactive compounds. Its unique structure and properties make it a valuable component in the creation of innovative pharmaceuticals and therapeutic agents.
Used in Research and Development:
In the scientific community, 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is used as a subject of research to explore its potential benefits and applications. Further studies are needed to understand its full potential and to unlock its capabilities in various fields of medicine and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 62414-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,1 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62414-75:
(7*6)+(6*2)+(5*4)+(4*1)+(3*4)+(2*7)+(1*5)=109
109 % 10 = 9
So 62414-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO7S/c1-6(14)18-9-4-17-12(13-5-21)11(20-8(3)16)10(9)19-7(2)15/h9-12H,4H2,1-3H3/t9-,10-,11+,12+/m1/s1

62414-75-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Sigma-Aldrich

  • (90245)  2,3,4-Tri-O-acetyl-α-D-arabinopyranosylisothiocyanate  for chiral derivatization, ≥98.0%

  • 62414-75-9

  • 90245-100MG

  • 1,353.69CNY

  • Detail

62414-75-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3R,4R,5S,6S)-4,5-diacetyloxy-6-isothiocyanatooxan-3-yl] acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62414-75-9 SDS

62414-75-9Relevant articles and documents

A simple method for the preparation of glycosyl isothiocyanates

Kuehne, Marco,Gyoergydeak, Zoltan,Lindhorst, Thisbe K.

, p. 949 - 951 (2007/10/03)

Glycosyl isothiocyanates became accessible from the corresponding peracetylated sugars in one step, by application of trimethylsilyl isothiocyanate and a Lewis acid in dichloromethane at room temperature. Georg Thieme Verlag Stuttgart.

Solvent-free preparation of glycosyl isothiocyanates

Lindhorst,Kieburg

, p. 1228 - 1230 (2007/10/02)

By a novel solvent-free procedure, peracetylated glycosyl bromides are reacted with potassium thiocyanate in the melt to give the corresponding glycosyl isothiocyanates. The method is applicable to several glycosyl bromides tested, including classical hexoses and pentoses, deoxy sugars and even disaccharides. No glycosyl thiocyanates are obtained. In general, the glycosyl isothiocyanates are formed stereoselectively having 1,2-trans configuration in yields between 41-74%.

STUDIES ON NUCLEOSIDE ANALOGS. XXIV. MONO- AND DISACCHARIDE ISOTHIOCYANATES

Ogura, Haruo,Takahashi, Hiroshi

, p. 87 - 90 (2007/10/02)

The reaction of mono- and disaccharide bromide with Pb(SCN)2 or AgSCN in dry benzene or benzene-toluene gives the respective mono- and disaccharide isothiocyanates and the confirmation of their stereochemistry of mono- and disaccharide isothiocyanates is

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 62414-75-9