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56-25-7 molecular structure
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(1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione

ChemBase ID: 132807
Molecular Formular: C10H12O4
Molecular Mass: 196.19988
Monoisotopic Mass: 196.07355886
SMILES and InChIs

SMILES:
C[C@@]12[C@@H]3CC[C@H]([C@@]1(C(=O)OC2=O)C)O3
Canonical SMILES:
O=C1OC(=O)[C@@]2([C@@]1(C)[C@@H]1CC[C@H]2O1)C
InChI:
InChI=1S/C10H12O4/c1-9-5-3-4-6(13-5)10(9,2)8(12)14-7(9)11/h5-6H,3-4H2,1-2H3/t5-,6+,9+,10-
InChIKey:
DHZBEENLJMYSHQ-XCVPVQRUSA-N

Cite this record

CBID:132807 http://www.chembase.cn/molecule-132807.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione
IUPAC Traditional name
cantharidin
Synonyms
Hexahydro-3a,7a-dimethyl-4,7-epoxyisobenzofuran-1,3-dione
Cantharidin
2,3-二甲基-7-氧杂-双环[2.2.1]庚烷-2,3-二羧酸酐
六氢-3α,7α-二甲基-4,7-环氧异苯并呋喃-1,3-二酮
班蝥酸酐
斑蝥素
CAS Number
56-25-7
EC Number
200-263-3
MDL Number
MFCD00134968
PubChem SID
162227084
24278334
PubChem CID
5944

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
C7632 external link Add to cart Please log in.
Data Source Data ID
PubChem 5944 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) 1.0591831  LogD (pH = 7.4) 1.0591831 
Log P 1.0591831  Molar Refractivity 45.4033 cm3
Polarizability 18.595083 Å3 Polar Surface Area 52.6 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Pharmacology Properties Bioassay(PubChem)
Solubility
DMSO: soluble expand Show data source
ethanol: soluble expand Show data source
Apperance
white expand Show data source
Melting Point
215-217 °C(lit.) expand Show data source
RTECS
RN8575000 expand Show data source
European Hazard Symbols
Highly toxic Highly toxic (T+) expand Show data source
UN Number
2811 expand Show data source
German water hazard class
3 expand Show data source
Hazard Class
6.1 expand Show data source
Packing Group
1 expand Show data source
Risk Statements
28-36/37/38 expand Show data source
Safety Statements
53-45 expand Show data source
GHS Pictograms
GHS06 expand Show data source
GHS Signal Word
Danger expand Show data source
GHS Hazard statements
H300-H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P264-P301 + P310-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges expand Show data source
RID/ADR
UN 2811 6.1/PG 1 expand Show data source
Gene Information
human ... PPP2CA(5515), PPP2CB(5516), PPP2CBP(5517), PPP2R1A(5518), PPP2R1B(5519), PPP2R2A(5520), PPP2R2B(5521), PPP2R2C(5522), PPP2R3A(5523), PPP2R5A(5525) expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - C7632 external link
Biochem/physiol Actions
蛋白磷酸酶 2A 的抑制剂。

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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