- 1-Chloroadamantane
-
- $5.00 / 1KG
-
2024-01-14
- CAS:935-56-8
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- 1-Chloroadamantane
-
- $0.00 / 1KG
-
2022-09-07
- CAS:935-56-8
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 1Ton
- 1-Chloroadamantane
-
- $0.10 / 1KG
-
2020-01-14
- CAS:935-56-8
- Min. Order: 1KG
- Purity: 99.0%
- Supply Ability: 1000 tons
|
| | 1-Chloroadamantane Basic information |
| | 1-Chloroadamantane Chemical Properties |
| Melting point | 165-166 °C(lit.) | | Boiling point | 211.58°C (rough estimate) | | density | 1.0492 (rough estimate) | | refractive index | 1.6012 (estimate) | | storage temp. | 2-8°C | | solubility | DMSO, Methanol (Slightly) | | form | Crystalline | | color | Off-White | | Water Solubility | Poorly soluble in water. Soluble in hydrocarbons. But readily soluble in nonpolar organic solvents. | | Stability: | Light Sensitive | | InChI | InChI=1S/C10H15Cl/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2 | | InChIKey | OZNXTQSXSHODFR-UHFFFAOYSA-N | | SMILES | C12(Cl)CC3CC(CC(C3)C1)C2 | | CAS DataBase Reference | 935-56-8(CAS DataBase Reference) | | NIST Chemistry Reference | Adamantane, 1-chloro-(935-56-8) | | EPA Substance Registry System | Tricyclo[3.3.1.13,7]decane, 1-chloro- (935-56-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 24/25 | | WGK Germany | 3 | | TSCA | Yes | | HS Code | 29035980 |
| | 1-Chloroadamantane Usage And Synthesis |
| Chemical Properties | white to light grey adhering crystalline solid or | | Uses | 1-Chloroadamantane was employed as precursor for the synthesis of perfluoroadmantane derivatives via aerosol direct fluorination. | | Uses | 1-Chloroadamantane, an adamantane derivative shown to exhibit virucidal activity against the Newcastle disease virus in chick embryo fibroblasts. (Adamantane EP Impurity A) | | Synthesis Reference(s) | Synthetic Communications, 19, p. 1697, 1989 DOI: 10.1080/00397918908051068 | | General Description | An unusual zwitterionic diradical intermediate complex was generated during the photoinduced electron-transfer substitution reaction between 1-chloroadamantane and tert-butylamine system in a hydrocarbon glass. | | Purification Methods | Crystallise the chloride from aqueous MeOH and sublime it at 100o/12torr. It also crystallises from MeOH at -70o. [Stetter et al. Chem Ber 92 1629 1959, Schleyer & Nicholas J Am Chem Soc 83 2700 1961, Beilstein 5 IV 469.] |
| | 1-Chloroadamantane Preparation Products And Raw materials |
|