1-Iodoadamantane

HCID 136609CAS 768-93-4

기본 정보

표준 SMILES
IC12CC3CC(CC(C3)C1)C2
InChIKey
PXVOATXCSSPUEM-UHFFFAOYSA-N
분자식
C10H15I
평균 분자량
262.13 g/mol
단동위원소 질량
262.02184848

이름 및 식별자

우선 이름
1-Iodoadamantane
IUPAC
1-iodoadamantane
영어명
1-Iodoadamantane
분자식
C10H15I
분자량
262.13

이름 및 동의어

1-Iodoadamantane768-93-4ADAMANTANE,1-JODOtricyclo[3.3.1.1~3,7~]decane, 1-iodo-DTXSID00227619NSC 169440tricyclo(3.3.1.1~3,7~)decane, 1-iodo-RefChem:76094DTXCID00150110InChI=1/C10H15I/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H1-Adamantyl iodideAdamantyl iodide
이름 더 보기
RARECHEM AQ TC 1020IFLAB-BB F0701-00781-Iodoadamantane 98%Adamantyl iodide,98%
Adamantane, 1-iodo-1-odoadamantane1-iodo-adamantane(3s,5s,7s)-1-iodoadamantaneMFCD00134444F0701-0078Tricyclo[3.3.1.13,7]decane, 1-iodo-C10H15I

데이터베이스 식별자

CAS
768-93-4
PubChem CID
136609
DTXSID
DTXSID00227619
Nikkaji
J329.828K

물성

구조 계산 물성

XLogP
4.4
극성 표면적
0 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
0
회전 가능 결합 수
0
무거운 원자 수
11

실험 및 물리화학적 성질

SpringerMaterials PropertiesSchoenflies notation

물리화학적 성질

녹는점
75 · 75-76 °C(lit.)
끓는 점
265.7 · 265.7±9.0℃ (760 Torr)
밀도
1.63 · 1.63±0.1 g/cm3 (20 ºC 760 Torr)
굴절률
1.661 · 1.6610 (estimate)
인화점
115.9 · 115.9±13.1℃
저장 조건
2 · 2-8°C(protect from light)

화학적 성질

solid

안전 및 규제

안전 데이터

wgk
3
스토리지 클래스
11 - Combustible Solids

화학 및 산업

응용 분야 · 2건

용도1-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 설명1-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.

공급사50 곳

上海康恩博医药科技有限公司17510465506 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
郑州阿尔法化工有限公司+86-18530059196 · [email protected]
湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
湖北万得化工有限公司15377098680 15377098680 · [email protected]

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