Angene Chemical
Draw
|
Currency :
Home Products

AG003P8W

464-49-3 | (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

Chemical structure of (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one, CAS 464-49-3
AG003P8W
sdsSDS
sdsCOA
TIP This product is typically in stock.Please contact us for quotation.
Request For Quotation

CAS Number 464-49-3
Catalog Number AG003P8W(AGN-PC-0OAJNE)
Chemical Name (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one
FEMA Number 2230
IUPAC Name (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
InChI InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m1/s1
InChI Key DSSYKIVIOFKYAU-XCBNKYQSSA-N
MDL Number MFCD00064149
Molecular Formula C10H16O
Molecular Weight 152.2334
NSC Number 755918
RTECS Number EX1260000
SMILES O=C1[C@](C2(C)C)(C)CC[C@]2([H])C1
UNII N20HL7Q941
Synonyms
camphora, D-CAMPHOR, (+)-Camphor, 464-49-3, (1R)-(+)-Camphor, (R)-Camphor, (+)-Bornan-2-one, (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, (R)-(+)-Camphor, (1R,4R)-camphor, Camphor(D), DL-Camphor, (+)-2-Bornanone, Camphora, D-(+)-Camphor, UNII-N20HL7Q941, Camphor (1R), d-2-Bornanone, Alcanfor, Japanese camphor, Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R,4R)-, CHEBI:15396, Camphor USP, Camphor, Racemic, d-2-Camphanone, DSSYKIVIOFKYAU-XCBNKYQSSA-N, N20HL7Q941, (1R)-Camphor, (1R,4R)-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one, NCGC00090681-04, Camphor, (+)-, DSSTox_CID_4721, D(+)-Camphor, 97%, DSSTox_RID_77510, DSSTox_GSID_24721, (1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one, Camphor oil, FEMA No. 2230, (1R,4R)-1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one, Huile de camphre, 2-Kamfanon, Kampfer [German], Camphor, D-, Camphor [USP], EINECS 207-355-2, UN2717, 2-Kamfanon [Czech], (+-)-Camphor, Caswell No. 155, CAS-464-49-3, AI3-01698, Huile de camphre [French], HSDB 37, Dextrocamphor, Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1R,4R)-, Natural camphor, Mulberry roots, EINECS 200-945-0, EINECS 244-350-4, MFCD00064149, Camphor D-form, EPA Pesticide Chemical Code 015602, Zang Qi, BRN 1907611, BRN 3196099, Cinnamomum camphora, 464-48-2, ( S)-camphor, d-Camphor [JAN], AI3-18783, Camphor, 96%, AC1Q2CCB, Spectrum2_000383, Spectrum3_000322, AC1L4L4L, SCHEMBL16069, BSPBio_001923, Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1theta)-, SPBio_000565, D-Camphor, >=97%, FG, CHEMBL504760, DTXSID4024721, BDBM36263, CTK7H1022, KBio3_001143, D-Camphor, natural, 96%, FG, Pharmakon1600-01500156, ZINC967520, (1R)-(+)-Camphor, 98%, HY-B1173, Tox21_110995, Tox21_202187, Tox21_303052, 5739AF, NSC755918, SBB012351, (+/-)-Camphor, >=95.5%, AKOS016001972, Tox21_110995_1, CS-4779, DB01744, NE11121, NSC-755918, RP21647, D-Camphor, analytical reference material, NCGC00090681-01, NCGC00090681-02, NCGC00090681-06, NCGC00090681-07, NCGC00090730-03, NCGC00257061-01, NCGC00259736-01, AJ-24527, CJ-04623, ST069333, ZB015454, (+/-)-Camphor, puriss., 96-101%, SBI-0206668.P002, ST24026081, EC 200-945-0, (+/-)-Camphor, SAJ first grade, >=96.0%, AB00443849_03, 0-07-00-00135 (Beilstein Handbook Reference), 4-07-00-00213 (Beilstein Handbook Reference), Camphor, synthetic [UN2717] [Flammable solid], (+/-)-Camphor, purum, synthetic, >=95.0% (GC), Camphor (dl), primary pharmaceutical reference standard, Z1741978849, UNII-5TJD82A1ET component DSSYKIVIOFKYAU-XCBNKYQSSA-N, Camphor, United States Pharmacopeia (USP) Reference Standard, (+)-Camphor, purum, natural, >=97.0% (sum of enantiomers, GC), Camphor (racemic), European Pharmacopoeia (EP) Reference Standard, D-Camphor, Pharmaceutical Secondary Standard; Certified Reference Material, (+/-)-Camphor, meets analytical specification of Ph.??Eur., BP, racemic, >=95% (GC), camphor, Formosa camphor, Laurel camphor, 2-Camphanone, Alphanon, Kampfer, 2-Bornanone, Sarna, Heet, Gum camphor, l-Camphor, Root bark oil, Matricaria camphor, Spirit of camphor, Bornan-2-one, Camphor, synthetic, trans-pi-oxocamphor, DL-Bornan-2-one, Bornane, 2-oxo-, Campho-Phenique Gel, (-)-Alcanfor, (+/-)-Camphor, Campho-Phenique Liquid, (-)-Bornan-2-one, SYNTHETIC CAMPHOR, (1R)-(+)-amphor, UNII-5TJD82A1ET, 1,7,7-Trimethylnorcamphor, 5TJD82A1ET, C10H16O, Campho-Phenique Cold Sore Gel, Camphor, (1R,4R)-(+)-, Fitzroys Barometer, solution A, Norcamphor, 1,7,7-trimethyl-, (+) - bornan - 2 - one, Camphor, (1S,4S)-(-)-, UNII-213N3S8275, 2-Keto-1,7,7-trimethylnorcamphane, EINECS 207-354-7, C10-H16-O, CID159055, MFCD00074738, NA2717, NSC 26351, ( inverted exclamation markA)-Camphor, 76-22-2, 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one, 1,7,7-Trimethylbicyclo(2.2.1)-2-heptanone, 1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one, (1R)-( )-Camphor, 98% - 100G 100g, Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1R)-, Bicyclo(2.2.1)heptane-2-one, 1,7,7-trimethyl-, Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1S)-, Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)-, Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-, Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1S,4S)-, Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S,4S)-, 21368-68-3, CAM,

Related Research Chemicals

    CERTIFICATE OF ANALYSIS
    Chemical Name: Batch Number:
    Chemical Structure: CAS Registry No:
    		Product ID:
    Manufacture Date:
    Storage Temperature:
    Formula:
    Molecular Weight:
    Quantity:
    Analysis Data:
    Test: Result:
    Conclusion: The above product meets the specifications of Angene.
    Analyst:Chase
    Date:
    Reviewed by:Jessie
    Date:
    Angene International Limited