1. Home
  2. [(2S)-6-methylhept-5-en-2-yl] acetate

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

[(2S)-6-methylhept-5-en-2-yl] acetate

CC(=CCCC(OC(=O)C)C)C Request for Quotation
Chemical Name: [(2S)-6-methylhept-5-en-2-yl] acetate
CAS Number: 19162-00-6
Product Number: AG001510(AGN-PC-005JYR)
Synonyms:
MDL No:
Molecular Formula: C10H18O2
Molecular Weight: 170.2487

Identification/Properties

Properties
BP:
178.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
170.252g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
170.131g/mol
Monoisotopic Mass:
170.131g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


6-Methylhept-5-en-2-yl acetate, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in organic chemistry, particularly in the creation of various fragrances and flavors. Its unique structure and reactivity make it a useful intermediate in the preparation of esters, alcohols, and ketones through acylation, alkylation, and condensation reactions.Its role in chemical synthesis extends to the production of pharmaceuticals, agrochemicals, and specialty chemicals. By incorporating 6-Methylhept-5-en-2-yl acetate into synthetic pathways, chemists can introduce specific functional groups and stereochemistry into their target molecules, enhancing their biological activity or physical properties. Additionally, this compound can act as a precursor for the synthesis of natural products and fine chemicals with complex structures.Overall, the application of 6-Methylhept-5-en-2-yl acetate in chemical synthesis allows for the efficient and selective construction of diverse molecules with tailored properties, making it an invaluable tool in the field of organic chemistry.