1-Iodoadamantane

1-Iodoadamantane 구조식 이미지
카스 번호:
768-93-4
상품명:
1-Iodoadamantane
동의어(영문):
NSC 169440;1-IODOADAMANTANE;Adamantyl iodide;1-Adamantyl iodide;RARECHEM AQ TC 1020;Adamantane, 1-iodo-;IFLAB-BB F0701-0078;1-Iodoadamantane 98%;(3s,5s,7s)-1-iodoadamantane;Andrographolide sodium bisulfite
CBNumber:
CB2191577
분자식:
C10H15I
포뮬러 무게:
262.13
MOL 파일:
768-93-4.mol
MSDS 파일:
SDS

1-Iodoadamantane 속성

녹는점
75-76 °C(lit.)
끓는 점
265.7±9.0℃ (760 Torr)
밀도
1.63±0.1 g/cm3 (20 ºC 760 Torr)
굴절률
1.6610 (estimate)
인화점
115.9±13.1℃
저장 조건
2-8°C(protect from light)
용해도
DMSO: 52 mg/mL (198.37 mM);;
안정성
안정적이지만 가볍고 습기에 민감합니다. 강한 산화제와 호환되지 않습니다.
InChI
InChI=1S/C10H15I/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2
InChIKey
PXVOATXCSSPUEM-UHFFFAOYSA-N
SMILES
C12(I)CC3CC(CC(C3)C1)C2

안전

WGK 독일 3

1-Iodoadamantane C화학적 특성, 용도, 생산

화학적 성질

solid

용도

1-Iodoadamantane is suitable reagent used to evaluate the rate constants for the reduction of haloadamantanes by SmI2 in presence of hexamethylphosphoramide (HMPA) and H2O by GC/MS-analyzed method. It may be used as iodine atom donor for probing the intermediacy of radical to investigate the chemistry of highly reactive, strained systems such as propellane. It may be used as starting reagent in the synthesis of N-(1-adamantyl)acetamide via nucleophilic substitution. It may be employed in the free-radical carbonylation reactions with alkenes.

일반 설명

1-Iodoadamantane is a haloadamantane. Voltammetric reduction of 1-iodoadamantane at a silver cathode in tetrahydrofuran (THF) and acetonitrile (ACN) is reported to involve a single electron forming a mixture of monomeric and dimeric products. The photoinduced reaction of 1-iodoadamantane in DMSO is reported to afford substitution products on C3, C6, and C8, 1-adamantanol, 1-adamantyl 2-naphthyl ether, and adamantine. The photostimulated reaction of the phthalimide anion with 1-iodoadamantane is reported to yield 3-(1-adamantyl) phthalimide and 4-(1-adamantyl) phthalimide, along with the reduction product adamantane. 1-Iodoadamantane is reported to undergoe photostimulated reaction with the enolate anion of acetone, acetophenone and propiophenone to give admantane and the substitution products.

Purification Methods

Dissolve the iodide in Et2O, shake with aqueous NaHSO3, aqueous K2CO3, and H2O, dry (Na2SO4), evaporate and recrystallise it from MeOH at -70o (to avoid alcoholysis) to give white crystals. [Schleyer & Nicholas J Am Chem Soc 83 2700 1961, lit m of 151-152.5o is incorrect.] Also purify by recrystallisation from pet ether (40-60oC) followed by rigorous drying and repeated sublimation. [Beilstein 5 IV 470.]

1-Iodoadamantane 준비 용품 및 원자재

원자재

준비 용품


1-Iodoadamantane 공급 업체

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