| Name | ascaridole |
|---|---|
| Synonyms |
ASCARIDOLE
Boldo ascidole 4-Isopropyl-1-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene 1,4-Peroxido-p-menthene-2 2,3-Dioxabicyclo(2.2.2)oct-5-ene, 1-isopropyl-4-methyl 2,3-Dioxabicyclo[2.2.2]oct-5-ene,1-Methyl-4-(1-Methylethyl) PA-MENTH-2-ENE,1,4-IDIOXY 1,4-epidioxy-p-menth-2-ene 1-Isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]octa-5-ene NSC-406266|||NSC 406266|||NSC Ascicum Askidol ASCIDOLE Kebal II cis-Ascaridole 1-isopropyl-4-methyl-7,8-dioxabicyclo[2.2.2]oct-2-ene 4-methyl-1-propan-2-yl-7,8-dioxabicyclo[2.2.2]oct-2-ene Ascidol Ascarisin 1,4-Peroxy-p-menth-2-ene Chenopodium oil (acetive component) Ascidiol Aslido Ascaridole0 nnDiscontiuned Unable to ship 1,4-idioxy-2-p-menthene 1-methyl-4-propan-2-yl-2,3-dioxabicyclo[2.2.2]oct-5-ene Uncinacina 1-methyl-4-(1-methylethyl)-2,3-dioxabicyclo[2.2.2]oct-5-ene p-Menth-2-ene, 1,4-idioxy Ascidole oxide 1-Isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene 6 2,3-Dioxabicyclo[2.2.2]oct-5-ene,1-methyl-4-(1-methylethyl) Ascaridol Ascapurin 1,4-idioxy-p-mentha-2-ene 1,4-idioxy-p-menth-2-ene Ascisin 1-Methyl-4-(1-methylethyl)-2,3-dioxabicyclo(2.2.2)oct-5-ene Ascaridiol Ascaricum Askaridol |
| Description | Ascaridole is an anthelmintic and also has antimalarial activity[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.051 g/cm3 |
|---|---|
| Boiling Point | 172.3ºC at 760 mmHg |
| Melting Point | 3.3ºC |
| Molecular Formula | C10H16O2 |
| Molecular Weight | 168.23 |
| Flash Point | 55.9ºC |
| Exact Mass | 168.11500 |
| PSA | 18.46000 |
| LogP | 2.45170 |
| Index of Refraction | 1.498 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| HS Code | 2932999099 |
|---|
|
~97%
512-85-6 |
| Literature: Ribeiro, Sonia M.; Serra, Armenio C.; Rocha Gonsalves, A.M.d'A. Tetrahedron, 2007 , vol. 63, # 33 p. 7885 - 7891 |
|
~76%
512-85-6 |
| Literature: Jary, Walther G.; Ganglberger, Thorsten; Poechlauer, Peter; Falk, Heinz Monatshefte fur Chemie, 2005 , vol. 136, # 4 p. 537 - 541 |
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~%
512-85-6 |
| Literature: Nardello, Veronique; Herve, Melanie; Alsters, Paul L.; Aubry, Jean-Marie Advanced Synthesis and Catalysis, 2002 , vol. 344, # 2 p. 184 - 191 |
|
~36%
512-85-6 |
| Literature: Nitz, Siegfried; Kollmannsberger, Hubert; Spraul, Martin H.; Drawert, Friedrich Phytochemistry (Elsevier), 1989 , vol. 28, # 11 p. 3051 - 3054 |
|
~38%
512-85-6 |
| Literature: Nitz, Siegfried; Kollmannsberger, Hubert; Spraul, Martin H.; Drawert, Friedrich Phytochemistry (Elsevier), 1989 , vol. 28, # 11 p. 3051 - 3054 |
|
~90%
512-85-6
Detail
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| Literature: Matusch, Rudolf; Schmidt, Gerhard Angewandte Chemie, 1988 , vol. 100, # 5 p. 729 - 730 |
|
~%
512-85-6 |
| Literature: Schenck; Gollnick Journal de Chimie Physique et de Physico-Chimie Biologique, 1958 , vol. 55, p. 892 |
|
~%
512-85-6 |
| Literature: Schenck et al. Justus Liebigs Annalen der Chemie, 1953 , vol. 584, p. 125,149 Full Text Show Details Schering A. G. Patent: DE752437 , 1941 ; DRP/DRBP Org.Chem. Full Text Show Details Schenck; Ziegler Naturwissenschaften, 1944 , vol. 32, p. 157 |
|
~%
512-85-6 |
| Literature: Schenck et al. Justus Liebigs Annalen der Chemie, 1953 , vol. 584, p. 125,149 Full Text Show Details Schering A. G. Patent: DE752437 , 1941 ; DRP/DRBP Org.Chem. Full Text Show Details Schenck; Ziegler Naturwissenschaften, 1944 , vol. 32, p. 157 |
| Precursor 6 | |
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| DownStream 10 | |
| HS Code | 2932999099 |
|---|---|
| Summary | 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |