641-74-7,MFCD10698761
Catalog No.:AA0034Z3

641-74-7 | (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%
in stock  
$6.00   $4.00
- +
10g
97%
in stock  
$8.00   $6.00
- +
25g
97%
in stock  
$19.00   $13.00
- +
100g
97%
in stock  
$72.00   $50.00
- +
500g
97%
in stock  
$200.00   $140.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0034Z3
Chemical Name:
(3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diol
CAS Number:
641-74-7
Molecular Formula:
C6H10O4
Molecular Weight:
146.1412
MDL Number:
MFCD10698761
SMILES:
O[C@@H]1CO[C@H]2[C@@H]1OC[C@H]2O
Properties
Properties
 
BP:
372.1°C at 760 mmHg  
Form:
Solid  
MP:
80-85 °C  
Refractive Index:
1.4128 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
122  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1.4  

Literature

Title: Isomannide derivatives as new class of inhibitors for human kallikrein 7.

Journal: Bioorganic & medicinal chemistry letters 20121001

Title: Renewable rigid diamines: efficient, stereospecific synthesis of high purity isohexide diamines.

Journal: ChemSusChem 20111216

Title: New chiral imidazolium ionic liquids from isomannide.

Journal: Carbohydrate research 20110201

Title: Pseudo-peptides derived from isomannide: inhibitors of serine proteases.

Journal: Amino acids 20100301

Title: Pseudo-peptides derived from isomannide as potential inhibitors of serine proteases.

Journal: Amino acids 20050601

Title: N- t-Boc-amino acid esters of isomannide. Potential inhibitors of serine proteases.

Journal: Amino acids 20041001

Quotation Request
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Additional Info:
SDS
Tags:641-74-7 Molecular Formula|641-74-7 MDL|641-74-7 SMILES|641-74-7 (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diol
Catalog No.: AA0034Z3
641-74-7,MFCD10698761
641-74-7 | (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diol
Pack Size: 5g
Purity: 97%
in stock
$6.00 $4.00
Pack Size: 10g
Purity: 97%
in stock
$8.00 $6.00
Pack Size: 25g
Purity: 97%
in stock
$19.00 $13.00
Pack Size: 100g
Purity: 97%
in stock
$72.00 $50.00
Pack Size: 500g
Purity: 97%
in stock
$200.00 $140.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0034Z3
Chemical Name: (3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diol
CAS Number: 641-74-7
Molecular Formula: C6H10O4
Molecular Weight: 146.1412
MDL Number: MFCD10698761
SMILES: O[C@@H]1CO[C@H]2[C@@H]1OC[C@H]2O
Properties
BP: 372.1°C at 760 mmHg  
Form: Solid  
MP: 80-85 °C  
Refractive Index: 1.4128 (estimate)  
Storage: Keep in dry area;Room Temperature;  
Complexity: 122  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 4  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1.4  
Literature fold

Title: Isomannide derivatives as new class of inhibitors for human kallikrein 7.

Journal: Bioorganic & medicinal chemistry letters20121001

Title: Renewable rigid diamines: efficient, stereospecific synthesis of high purity isohexide diamines.

Journal: ChemSusChem20111216

Title: New chiral imidazolium ionic liquids from isomannide.

Journal: Carbohydrate research20110201

Title: Pseudo-peptides derived from isomannide: inhibitors of serine proteases.

Journal: Amino acids20100301

Title: Pseudo-peptides derived from isomannide as potential inhibitors of serine proteases.

Journal: Amino acids20050601

Title: N- t-Boc-amino acid esters of isomannide. Potential inhibitors of serine proteases.

Journal: Amino acids20041001

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