Diaceton-alpha-D-mannofuranose CAS 14131-84-1
Identification
Properties
Safety Data
Specifications & Other Information
Links
Identification
CAS Number
14131-84-1
Name
Diaceton-alpha-D-mannofuranose
Synonyms
(3aS,4S,6R,6aS)-6-[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol [ACD/IUPAC Name]
(3aS,4S,6R,6aS)-6-[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol [German] [ACD/IUPAC Name]
(3aS,4S,6R,6aS)-6-[(4R)-2,2-Diméthyl-1,3-dioxolan-4-yl]-2,2-diméthyltétrahydrofuro[3,4-d][1,3]dioxol-4-ol [French] [ACD/IUPAC Name]
2,3:5,6-Di-O-isopropylidene-a-D-mannofuranose
(+)-2,3:5,6-Di-O-isopropylidene-α-D-mannofuranose
(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol
(3aS,4S,6R,6aS)-6-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol
[14131-84-1]
14131-84-1 [RN]
2,3:5,6-Di-O-isopropylidene-a
2,3:5,6-Di-O-isopropylidene-α-D-mannofuranose
2,3:5,6-Di-O-isopropylidene-α-D-mannofuranose
2,3:5,6-DI-O-ISOPROPYLIDENE-α-D-MANNOFURANOSE
78573-85-0 [RN]
Diacetone-D-mannose
Diaceton-α-D-mannofuranose
MFCD00134206 [MDL number]
OR-3791
Molecular Structure
SMILES
CC1(OC[C@@H](O1)[C@@H]2[C@H]3[C@@H]([C@H](O2)O)OC(O3)(C)C)C
StdInChI
InChI=1S/C12H20O6/c1-11(2)14-5-6(16-11)7-8-9(10(13)15-7)18-12(3,4)17-8/h6-10,13H,5H2,1-4H3/t6-,7-,8+,9+,10+/m1/s1
StdInChIKey
JWWCLCNPTZHVLF-ZJDVBMNYSA-N
Molecular Formula
C12H20O6
Molecular Weight
260.29
Beilstein Registry Number
84382
MDL Number
MFCD00134206
Properties
Appearance
White crystalline power
Safety Data
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RIDADR
NONH for all modes of transport
WGK Germany
3
Specifications and Other Information of Our Diaceton-alpha-D-mannofuranose CAS 14131-84-1
Standard
Enterprise standard
Identification Methods
HPLC
Purity
98%min
Heavy Metals
20ppm max
Loss on Drying
1%max
Residue on Ignition
0.5% max
Package
According to customer requirements to packaging
Storage
Under the room temperature and away from light
Application
Synthesis of fake eggs scattered bag streptozotocin and doxorubicin lead to nuclear sugar mannose protected intermediate.
Links
Ulcho Biochemical Ltd
This product is developed by our sub R&D company Ulcho Biochemical Ltd, and please click the link below for details.
http://www.ulcho.com/diaceton-alpha-d-mannofuranose-cas-14131-84-1/
Watson International Ltd
This product is sold exclusively through our sales company Watson International Ltd, and please click the link below for details.
http://www.watson-int.com/diaceton-alpha-d-mannofuranose-cas-14131-84-1/