Product Name

  • Name

    Norcantharidin

  • EINECS 637-280-4
  • CAS No. 5442-12-6
  • Article Data9
  • CAS DataBase
  • Density 1.468 g/cm3
  • Solubility
  • Melting Point 110 °C
  • Formula C8H8O4
  • Boiling Point 362.464 °C at 760 mmHg
  • Molecular Weight 168.149
  • Flash Point 167.017 °C
  • Transport Information
  • Appearance solid
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 5442-12-6 (Norcantharidin)
  • Hazard Symbols
  • Synonyms 7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylicanhydride (8CI);4,10-Dioxatricyclo[5.2.1.02,6]decane-3,5-dione;NSC 14003;4,7-Epoxyisobenzofuran-1,3-dione,hexahydro-;
  • PSA 52.60000
  • LogP -0.13660

Synthetic route

endo-7-oxabicyclo<2.2.1>heptane-2,3-dicarboxylic acid
28871-63-8

endo-7-oxabicyclo<2.2.1>heptane-2,3-dicarboxylic acid

endothall anhydride
5442-12-6

endothall anhydride

Conditions
ConditionsYield
In acetyl chloride99%
7-oxanorborn-5-ene-2,3-dicarboxylic anhydride
5426-09-5

7-oxanorborn-5-ene-2,3-dicarboxylic anhydride

endothall anhydride
5442-12-6

endothall anhydride

Conditions
ConditionsYield
With hydrogen; palladium 10% on activated carbon In ethyl acetate for 16h; Heating / reflux;98%
With palladium 10% on activated carbon; hydrogen In ethyl acetate at 20℃; for 24h;97%
With hydrogen In ethyl acetate at 280℃;81%
methanol
67-56-1

methanol

endothall anhydride
5442-12-6

endothall anhydride

3-(methoxycarbonyl)-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid
57105-58-5

3-(methoxycarbonyl)-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid

Conditions
ConditionsYield
at 60℃; for 16h;98%
for 3h; Heating / reflux;96%
at 80 - 85℃; for 3.5h;72.2%
at 80 - 85℃; for 15.5h; Cooling;24.2%
endothall anhydride
5442-12-6

endothall anhydride

ethanol
64-17-5

ethanol

7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid monoethyl ester
115122-59-3

7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid monoethyl ester

Conditions
ConditionsYield
at 80℃; for 4.5h;87%
at 80℃; for 4.5h;87%
2-azido-1-azidomethyl ethylamine
921607-52-5

2-azido-1-azidomethyl ethylamine

endothall anhydride
5442-12-6

endothall anhydride

C11H15N7O4

C11H15N7O4

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 60℃; for 24h; Inert atmosphere;84%
endothall anhydride
5442-12-6

endothall anhydride

N,N-dimethylethylenediamine
108-00-9

N,N-dimethylethylenediamine

1-N-(3-exocarboxy-7-oxabicyclo[2.2.1]heptane-2-exocarbonyl)amino-2-(N,N-dimethyl)aminoethane

1-N-(3-exocarboxy-7-oxabicyclo[2.2.1]heptane-2-exocarbonyl)amino-2-(N,N-dimethyl)aminoethane

Conditions
ConditionsYield
In toluene for 2h; Heating / reflux;74%
endothall anhydride
5442-12-6

endothall anhydride

benzyl alcohol
100-51-6

benzyl alcohol

7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, mono (phenylmethyl)ester
140486-19-7

7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, mono (phenylmethyl)ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 160℃; for 6h;71.2%
endothall anhydride
5442-12-6

endothall anhydride

1-t-Butoxycarbonylpiperazine
57260-71-6

1-t-Butoxycarbonylpiperazine

4-(3-carboxy-7-oxa-bicyclo[2.2.1]heptane-2-carbonyl)piperazine-1-carboxylic acid tert-butyl ester
1047659-23-3

4-(3-carboxy-7-oxa-bicyclo[2.2.1]heptane-2-carbonyl)piperazine-1-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
In toluene at 100 - 110℃; for 8h;47%
In toluene at 100℃; for 8h;
endothall anhydride
5442-12-6

endothall anhydride

A

phthalic anhydride
85-44-9

phthalic anhydride

B

benzene
71-43-2

benzene

Conditions
ConditionsYield
With zeolite Y with a silica-alumina at 200℃; Inert atmosphere;A 41%
B 23%
endothall anhydride
5442-12-6

endothall anhydride

4-amino-1-(2-(4-methoxyphenyl)ethyl)piperidine
85098-70-0

4-amino-1-(2-(4-methoxyphenyl)ethyl)piperidine

3-{1-[2-(4-methoxy-phenyl)-ethyl]piperidin-4-ylcarbamoyl}-7-oxa-bicyclo[2.2.1]-heptane-2-carboxylic acid
1047659-20-0

3-{1-[2-(4-methoxy-phenyl)-ethyl]piperidin-4-ylcarbamoyl}-7-oxa-bicyclo[2.2.1]-heptane-2-carboxylic acid

Conditions
ConditionsYield
In toluene at 100℃; for 20h;36%
endothall anhydride
5442-12-6

endothall anhydride

2-fluorobenzyl alcohol
446-51-5

2-fluorobenzyl alcohol

C15H15FO5

C15H15FO5

Conditions
ConditionsYield
With dmap In dichloromethane at 60℃; for 14h; Sealed tube; Inert atmosphere;34.7%
endothall anhydride
5442-12-6

endothall anhydride

3-fluoro-benzenemethanol
456-47-3

3-fluoro-benzenemethanol

C15H15FO5

C15H15FO5

Conditions
ConditionsYield
With dmap In dichloromethane at 60℃; for 14h; Sealed tube; Inert atmosphere;30.7%
endothall anhydride
5442-12-6

endothall anhydride

A

phthalic anhydride
85-44-9

phthalic anhydride

B

C8H8O4

C8H8O4

Conditions
ConditionsYield
With zeolite Y with a silica-alumina at 160℃; for 15h; Inert atmosphere;A 15%
B 28%
4-fluorobenzylic alcohol
459-56-3

4-fluorobenzylic alcohol

endothall anhydride
5442-12-6

endothall anhydride

C15H15FO5

C15H15FO5

Conditions
ConditionsYield
With dmap In dichloromethane at 60℃; for 14h; Sealed tube; Inert atmosphere;25.2%
2-amino-1,3-oxazole
4570-45-0

2-amino-1,3-oxazole

endothall anhydride
5442-12-6

endothall anhydride

2-oxazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione
16131-79-6

2-oxazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione

2-thiazolylamine
96-50-4

2-thiazolylamine

endothall anhydride
5442-12-6

endothall anhydride

2-thiazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione
16131-73-0

2-thiazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione

3(5)-amino-1,2,4-triazole
61-82-5

3(5)-amino-1,2,4-triazole

endothall anhydride
5442-12-6

endothall anhydride

2-(1H-[1,2,4]triazol-3-yl)-hexahydro-4,7-epioxido-isoindole-1,3-dione
19691-96-4

2-(1H-[1,2,4]triazol-3-yl)-hexahydro-4,7-epioxido-isoindole-1,3-dione

Conditions
ConditionsYield
In N,N-dimethyl-formamide
2-amino-5,6-dimethylbenzothiazole
29927-08-0

2-amino-5,6-dimethylbenzothiazole

endothall anhydride
5442-12-6

endothall anhydride

2-(5,6-dimethyl-benzothiazol-2-yl)-hexahydro-4,7-epioxido-isoindole-1,3-dione
16131-78-5

2-(5,6-dimethyl-benzothiazol-2-yl)-hexahydro-4,7-epioxido-isoindole-1,3-dione

2-Amino-6-ethoxybenzothiazole
94-45-1

2-Amino-6-ethoxybenzothiazole

endothall anhydride
5442-12-6

endothall anhydride

2-(6-ethoxy-benzothiazol-2-yl)-hexahydro-4,7-epioxido-isoindole-1,3-dione
16131-62-7

2-(6-ethoxy-benzothiazol-2-yl)-hexahydro-4,7-epioxido-isoindole-1,3-dione

2-Amino-6-ethoxybenzothiazole
94-45-1

2-Amino-6-ethoxybenzothiazole

endothall anhydride
5442-12-6

endothall anhydride

3-(6-ethoxy-benzothiazol-2-ylcarbamoyl)-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid

3-(6-ethoxy-benzothiazol-2-ylcarbamoyl)-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid

Conditions
ConditionsYield
In dichloromethane
naphtho[2,3-d]thiazole-2-amine
39608-20-3

naphtho[2,3-d]thiazole-2-amine

endothall anhydride
5442-12-6

endothall anhydride

2-naphtho[2,3-d]thiazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione
19783-66-5

2-naphtho[2,3-d]thiazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione

naphtho[2,3-d]thiazole-2-amine
39608-20-3

naphtho[2,3-d]thiazole-2-amine

endothall anhydride
5442-12-6

endothall anhydride

3-naphtho[2,3-d]thiazol-2-ylcarbamoyl-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid
19692-05-8

3-naphtho[2,3-d]thiazol-2-ylcarbamoyl-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid

Conditions
ConditionsYield
In dichloromethane
endothall anhydride
5442-12-6

endothall anhydride

naphthalen-2-ylamine
91-59-8

naphthalen-2-ylamine

(3aα,4α,7α,7aα)-Hexahydro-2-(2-naphthalenyl)-4,7-epoxy-1H-isoindole-1,3(2H)-dione
406220-74-4

(3aα,4α,7α,7aα)-Hexahydro-2-(2-naphthalenyl)-4,7-epoxy-1H-isoindole-1,3(2H)-dione

Conditions
ConditionsYield
In water; acetic acid65.7 mg (0.224 mmol, 74.7%)
endothall anhydride
5442-12-6

endothall anhydride

7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, mono (phenylmethyl)ester
140486-19-7

7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, mono (phenylmethyl)ester

Conditions
ConditionsYield
With benzyl alcohol2.7 g (33%)
endothall anhydride
5442-12-6

endothall anhydride

sodium sulfate
7757-82-6

sodium sulfate

cis-endo-2,3-(bishydroxymethyl)-7-oxabicyclo<2.2.1>heptane
68940-53-4

cis-endo-2,3-(bishydroxymethyl)-7-oxabicyclo<2.2.1>heptane

Conditions
ConditionsYield
In tetrahydrofuran
In tetrahydrofuran
endothall anhydride
5442-12-6

endothall anhydride

(exo)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one
6253-21-0

(exo)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one

Conditions
ConditionsYield
With sodium borohydrid In tetrahydrofuran; hydrogenchloride; dichloromethane
C6H14N4O6Pt

C6H14N4O6Pt

endothall anhydride
5442-12-6

endothall anhydride

C14H22N2O5Pt

C14H22N2O5Pt

Conditions
ConditionsYield
With sodium hydroxide In water at 20℃; for 16h;
endothall anhydride
5442-12-6

endothall anhydride

Conditions
ConditionsYield
With sodium hydroxide In water

Norcantharidin Specification

The Norcantharidin, with the CAS registry number 5442-12-6, is also known as 7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic anhydride. It belongs to the product categories of Norbornene Derivatives; Plant extract. This chemical's molecular formula is C8H8O4 and molecular weight is 168.15. What's more, its systematic name is 4,10-Dioxatricyclo[5.2.1.02,6]decane-3,5-dione. It is used as antineoplastic agents.

Physical properties of Norcantharidin are: (1)ACD/LogP: -0.971; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -0.97; (4)ACD/LogD (pH 7.4): -0.97; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 7.06; (8)ACD/KOC (pH 7.4): 7.06; (9)#H bond acceptors: 4; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 52.6 Å2; (13)Index of Refraction: 1.55; (14)Molar Refractivity: 36.47 cm3; (15)Molar Volume: 114.53 cm3; (16)Polarizability: 14.458×10-24cm3; (17)Surface Tension: 50.12 dyne/cm; (18)Density: 1.468 g/cm3; (19)Flash Point: 167.017 °C; (20)Enthalpy of Vaporization: 60.841 kJ/mol; (21)Boiling Point: 362.464 °C at 760 mmHg; (22)Vapour Pressure: 0 mmHg at 25°C.

You can still convert the following datas into molecular structure:
(1)SMILES: C1CC2C3C(C1O2)C(=O)OC3=O
(2)Std. InChI: InChI=1S/C8H8O4/c9-7-5-3-1-2-4(11-3)6(5)8(10)12-7/h3-6H,1-2H2
(3)Std. InChIKey: JAABVEXCGCXWRR-UHFFFAOYSA-N 

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous 10mg/kg (10mg/kg)   U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#05066.

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