185021-11-8

• 

• Basic information

  1. Product Name: D-arabino-Hexitol, 2-amino-1,5-anhydro-2,3-dideoxy- (9CI)
  2. Synonyms: D-arabino-Hexitol, 2-amino-1,5-anhydro-2,3-dideoxy- (9CI)
  3. CAS NO:185021-11-8
  4. Molecular Formula: C6H13NO3
  5. Molecular Weight: 147.17232
  6. EINECS: N/A
  7. Product Categories: AMINEPRIMARY
  8. Mol File: 185021-11-8.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: D-arabino-Hexitol, 2-amino-1,5-anhydro-2,3-dideoxy- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: D-arabino-Hexitol, 2-amino-1,5-anhydro-2,3-dideoxy- (9CI)(185021-11-8)
  11. EPA Substance Registry System: D-arabino-Hexitol, 2-amino-1,5-anhydro-2,3-dideoxy- (9CI)(185021-11-8)

• 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: 185021-11-8(Hazardous Substances Data)

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185021-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185021-11-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,0,2 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 185021-11:
(8*1)+(7*8)+(6*5)+(5*0)+(4*2)+(3*1)+(2*1)+(1*1)=108
108 % 10 = 8
So 185021-11-8 is a valid CAS Registry Number.

185021-11-8Upstream product

• 150653-80-8 Methanesulfonic acid (2R,4aR,7R,8aS)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 149312-20-9 1',5'-anhydro-4,6-O-benzylidene-3-deoxy-D-glucitol 

185021-11-8Downstream Products

185021-11-8Relevant articles and documents

The synthesis of modified D- and L-anhydrohexitol nucleosides

Andersen, Marc W.,Daluge, Susan M.,Kerremans, Luk,Herdewijn, Piet

, p. 8147 - 8150 (2007/10/03)

The synthesis and antiviral activities of novel L-isomers 9-13 and modified D-guanine analogs 1d,e of recently reported anhydrohexitol nucleosides 1 are described. An efficient approach to known anhydrohexitol nucleoside precursor 2 from diacetone-D-glucose 3 is also reported.

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