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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Cyclopropanecarboxylic acid, anhydride

O=C(C1CC1)OC(=O)C1CC1 Request for Quotation
Chemical Name: Cyclopropanecarboxylic acid, anhydride
CAS Number: 33993-24-7
Product Number: AG00I6PS(AGN-PC-0JPFLL)
Synonyms:
MDL No:
Molecular Formula: C8H10O3
Molecular Weight: 154.1632

Identification/Properties

Computed Properties
Molecular Weight:
154.165g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
154.063g/mol
Monoisotopic Mass:
154.063g/mol
Topological Polar Surface Area:
43.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
179
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Cyclopropanecarboxylic acid anhydride is a versatile chemical reagent commonly used in organic synthesis. This compound serves as a valuable building block in the creation of various functionalized organic molecules due to its unique structural features and reactivity. In chemical synthesis, cyclopropanecarboxylic acid anhydride can undergo nucleophilic addition reactions with various nucleophiles such as amines, alcohols, and thiols to introduce cyclopropane rings into target molecules. This process enables the formation of complex cyclic structures and facilitates the synthesis of bioactive compounds, pharmaceuticals, and materials with specific properties. Furthermore, the reactivity of cyclopropanecarboxylic acid anhydride can be tuned and controlled by adjusting reaction conditions, making it a valuable tool for chemists seeking to design and create novel molecular structures in their synthetic endeavors.