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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)-

5-Norbornene-2-carboxylic acid (8CI)

OC(=O)C1CC2CC1C=C2 Request for Quotation
Chemical Name: 5-Norbornene-2-carboxylic acid (8CI)
CAS Number: 120-74-1
Product Number: AG000Q1N(AGN-PC-0DA1ZV)
Synonyms:
MDL No:
Molecular Formula: C8H10O2
Molecular Weight: 138.1638

Identification/Properties

Properties
MP:
34-42 °C
BP:
136-138 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.494(lit.)
Computed Properties
Molecular Weight:
138.166g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
138.068g/mol
Monoisotopic Mass:
138.068g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
195
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
3
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:
P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid is a versatile compound widely utilized in chemical synthesis as a key building block for the creation of various organic molecules. With its unique bicyclic structure, this acid serves as a valuable starting material in the preparation of pharmaceuticals, agrochemicals, and advanced materials. By undergoing strategic chemical transformations, Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid can be modified to introduce specific functional groups, enabling the synthesis of diverse compounds with tailored properties and applications. Its role in chemical synthesis highlights its significant contribution to the advancement of modern chemistry and the development of innovative products across industries.