19165-06-1

• 

• Basic information

  1. Product Name: 2-deoxy-L-fucose
  2. Synonyms: 2-deoxy-L-fucose
  3. CAS NO:19165-06-1
  4. Molecular Formula: C₆H₁₂O₄
  5. Molecular Weight: 148.16
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 19165-06-1.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 365.9°Cat760mmHg
  3. Flash Point: 189.3°C
  4. Appearance: /
  5. Density: 1.249g/cm³
  6. Vapor Pressure: 7.73E-07mmHg at 25°C
  7. Refractive Index: 1.494
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-deoxy-L-fucose(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-deoxy-L-fucose(19165-06-1)
  12. EPA Substance Registry System: 2-deoxy-L-fucose(19165-06-1)

• 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: 19165-06-1(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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  Cas No: 19165-06-1

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19165-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19165-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,6 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19165-06:
(7*1)+(6*9)+(5*1)+(4*6)+(3*5)+(2*0)+(1*6)=111
111 % 10 = 1
So 19165-06-1 is a valid CAS Registry Number.

InChI:InChI=1/C6H12O4/c1-4(8)6(10)5(9)2-3-7/h3-6,8-10H,2H2,1H3/t4-,5-,6+/m0/s1

19165-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	L-lyxo-2,6-dideoxy-hexose

1.2 Other means of identification

Product number	-
Other names	L-lyxo-2,6-Didesoxy-hexose

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:19165-06-1 SDS

19165-06-1Upstream product

• 77210-24-3 methyl 2,6-dideoxy-α-D-xylo-hexopyranoside 
• 104048-37-5 ((E)-5-Propenyl)-4,5-dihydro-isoxazole 
• 104048-44-4 (1R,2S)-(S)-1-(4,5-Dihydro-isoxazol-5-yl)-propane-1,2-diol 
• 104048-44-4 (1S,2R)-(S)-1-(4,5-Dihydro-isoxazol-5-yl)-propane-1,2-diol 
• 14711-68-3 methyl-[bis-O-(toluene-4-sulfonyl)-α-D-xylo-2,6-dideoxy-hexopyranoside] 
• 67308-47-8 methyl-(α-D-xylo-2-deoxy-hexopyranoside) 
• 897959-06-7 methyl-[tris-O-(toluene-4-sulfonyl)-α-D-xylo-2-deoxy-hexopyranoside] 

19165-06-1Downstream Products

19165-06-1Relevant articles and documents

-

Iselin,Reichstein

, p. 1203,1207 (1944)

-

SILYL NITRONATES AND NITRILE OXIDES IN ORGANIC SYNTHESIS. A NOVEL ROUTE TO D,L-DEOXYSUGARS. USE OF ALUMINIUM OXIDE AS SOLID PHASE BASE FOR GENERATION OF NITRILE OXIDES FROM HYDROXIMIC ACID CHLORIDES

Torssell, K. B. G.,Hazell, A. C.,Hazell, R. G.

, p. 5569 - 5576 (2007/10/02)

Novel methodology is developed for a three step synthesis of deoxyaldoses and deoxyketoses. 1.Regioselective addition of silyl nitronate or nitrile oxide to a diene. 2.Stereospecific hydroxylation of the double bond. 3.Unmasking of the aldol moiety by catalytic reduction of the 2-isoxazoline.The syntheses of D.L-deoxyribose, D,L-oleose, D,L-digitoxose, D,L-2-deoxygalactose, 1,3-dideoxyfructose, 3-deoxyfructose etc. are described.Basic aluminium oxide is introduced as a solid phase base for the one step synthesis of 2-isoxazolines from aldoximes and olefins.An X-ray diffraction study of compound 13c verifies the stereochemical assignments.

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