1-アダマンタンカルボン酸

1-Adamantanecarboxylic acid

HCID 13235CAS 15897-81-1

基本情報

標準SMILES
O=C(O)C12CC3CC(CC(C3)C1)C2
InChIKey
JIMXXGFJRDUSRO-UHFFFAOYSA-N
分子式
C11H16O2
平均分子量
180.24 g/mol
単同位体質量
180.11502975

名称と識別子

優先名称
1-Adamantanecarboxylic acid
IUPAC
adamantane-1-carboxylic acid
現地名
1-アダマンタンカルボン酸
英語名
1-Adamantanecarboxylic acid
分子式
C11H16O2
分子量
180.24

名称と別名

1-Adamantanecarboxylic acid828-51-3Adamantoic acidAdamantanecarboxylic acidRefChem:552944DTXCID101505931DTXSID901020894212-584-6Adamantane-1-carboxylic acid1-Carboxyadamantane1-adamantane carboxylic acidMFCD00074720
名称をさらに表示
1-アダマンタンカルボン酸アダマンタン-1-カルボン酸トリシクロ[3.3.1.13,7]デカン-1-カルボン酸アダマンタン-3-カルボン酸1‐アダマンタンカルボン酸アダマント酸アダマンタン3-カルボン酸5-アダマンタンカルボン酸1-Adamantyl Carboxylic Acid1-AdamantanecarboxyL1-AdamantanecarboxylicAdamantane-1-carboxylic acid 99%Saxaint-KAKOS BC-06551-ADAMANTOIC ACID
3-ADAMANTANECARBOXYLIC ACIDadamantane carboxylic acidCHEMBL1705681-Adamantane-1-carboxylic acidtricyclo[3.3.1.1~3,7~]decane-1-carboxylic acid(3r,5r,7r)-adamantane-1-carboxylic acidTricyclo[3.3.1.13,7]decane-1-carboxylic acidadamantane-carboxylic acid

データベース識別子

CAS
15897-81-1、828-51-3
PubChem CID
13235
DTXSID
DTXSID40870784
ChEMBL
CHEMBL170568、CHEMBL5186120
EC Number
212-584-6
Nikkaji
J108B

物性

構造計算による物性

XLogP
2.6
極性表面積
37.3 Ų
水素結合供与体数
1
水素結合受容体数
2
回転可能結合数
1
重原子数
13

実験および物理化学的性質

Chemical ClassesOther Classes -> Organic Acids
Physical DescriptionWhite powder; [Alfa Aesar MSDS]

物理化学的性質

融点
172 · 172-174 °C (lit.)
沸点
253.08 °C · 253.08°C (rough estimate)
比重(密度)
0.9976 · 0.9976 (rough estimate)
屈折率
1.491 · 1.4910 (estimate)
貯蔵温度
Sealed in dry,Room Temperature
溶解性
クロロホルム、メタノール(微量)

化学的性質

化学的特性white to off-white crystalline powder

安全と法規制

GHS分類

GHS Classification · 4 件

Warning

H302 (28.6%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 14 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory Information · 2 件

Status: Active Update: 29-05-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/23651

Tricyclo3.3.1.13,7decane-1-carboxylic acid: Does not have an individual approval but may be used under an appropriate group standard

Hazards SummaryIntraperitoneal lethal-dose (mouse) >600 mg/kg; Causes anticonvulsant behavior in lethal-dose studies of mice (route unreported); [RTECS] A skin and strong eye irritant; [Alfa Aesar MSDS]
Hazard Classes and CategoriesAcute Tox. 4 (28.6%)

安全データ

wgk
3
rtecs
AU4452200
hs_code
29162000
risk_code
36/37/38
hazard_code
Xi
hazard_note
Irritant

化学と産業

応用分野 · 1 件

使用1-Adamantanecarboxylic acid can be used as: A stabilizer in the synthesis of monodisperse, highly crystalline CoPt3nanoparticles and porous platinum nanoparticles.An additive in polycondensation reactions to yield conjugated polymers as possible optoelectronic materials.An additive in the allylic substitution reaction, which is catalyzed by palladium in an aqueous medium.

調製方法 · 1 件

純化方法Possible impurities are trimethylacetic acid and C9 and C13 acids. Dissolve 15g of the acid in CCl4 (300mL) and shake with 110mL of 15N aqueous NH3 whereby the ammonium salt separates and is collected. Acid impurities form soluble ammonium salts. The salt is washed with cold Me2CO (20mL) and suspended in H2O (250mL). This is treated with 12N HCl and extracted with CHCl3 (100mL). The dried (Na2SO4) extract was evaporated and the residue was recrystallised from a mixture of MeOH (30mL) and H2O (ca 10mL) to give the pure acid (10-11g). [Koch & Haaf Org Synth Coll Vol V 20 1973.] It was also recrystallised from absolute EtOH and dried under vacuum at 100o. Alternatively, the acid (5g) is refluxed for 2hours with 15mL of MeOH and 2mL of 98% H2SO4 (cool when mixing this solution). Pour into 10 volumes of H2O and extract with the minimum volume of CHCl3 to give clear separation of phases. The extract is washed with H2O, dried (CaCl2) and distilled. The methyl ester is collected at 77-79o/1mm, m 38-39o. The ester is hydrolysed with the calculated amount of N KOH and refluxed until clear. Acidification with HCl provides the pure acid with 90% recovery. The amide crystallises from cyclohexane, m 189o. [Stetter et al. Chem Ber 92 1629 1959.] [Beilstein 9 IV 253.]

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関連反応

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