基本情報
- 標準SMILES
NC(=O)OCc1ccccc1- InChIKey
PUJDIJCNWFYVJX-UHFFFAOYSA-N- 分子式
- C8H9NO2
- 平均分子量
- 151.16 g/mol
- 単同位体質量
- 151.06332853
名称と識別子
- 優先名称
- Benzyl carbamate
- IUPAC
- benzyl carbamate
- 現地名
- カルバミン酸ベンジル
- 英語名
- Benzyl carbamate
- 分子式
- C8H9NO2
- 分子量
- 151.16
名称と別名
名称をさらに表示
データベース識別子
- CAS
621-84-1- PubChem CID
- 12136
- DTXSID
DTXSID00211159- ChEMBL
CHEMBL2259788- UNII
- 7890Q001S7
- EC Number
- 210-710-4
- Nikkaji
- J95.774G
物性
構造計算による物性
- XLogP
- 1.2
- 極性表面積
- 52.3 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
- 3
- 重原子数
- 11
- 形式電荷
- 0
- 複雑度
- 130
物理化学的性質
- 融点
- 86 · 86-89 °C (lit.)
- 沸点
- 273.17 °C · 273.17°C (rough estimate)
- 比重(密度)
- 1.2023 · 1.2023 (rough estimate)
- 屈折率
- 1.581 · 1.5810 (estimate)
- 貯蔵温度
- Keep in dark place,Sealed in dry,Room Temperature
- 溶解性
- クロロホルム(微量)、メタノール(微量)
- 外見
- パウダーまたはフレーク
- 酸解離定数(Pka)
- 13.42 · 13.42±0.50(Predicted)
- 色
- オフホワイトからライトベージュ
- 水溶解度
- 68.02 g/L · 68.02g/L(37℃)
- BRN
- 1865635 · 1865635
- InChI
- InChI=1S/C8H9NO2/c9-8(10)11-6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)
- InChIKey
- PUJDIJCNWFYVJX-UHFFFAOYSA-N
- SMILES
- C(OCC1=CC=CC=C1)(=O)N
- CAS データベース
- 621 · 621-84-1(CAS DataBase Reference)
- NISTの化学物質情報
- Carbamic acid, benzyl ester(621-84-1)
化学的性質
化学的特性Off-white to light beige powder or flakes, melting point 87-89 ℃. Insoluble in water, soluble in organic solvents such as benzene.
安全と法規制
GHS分類
GHS Classification
Warning
H302 (50%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P273, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, 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 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
安全データ
- wgk
- 3
- hs_code
- 29242995
- risk_code
- 20/21/22-36/37/38
- hazard_code
- Xn
- safety_code
- 22-24/25-36-26
- ストレージクラス
- 11 - Combustible Solids
化学と産業
応用分野
用途有機合成原料。
使用Benzyl carbamate is a reagent used for the nucleophilic introduction of an amino-protected group, Benzyl carbamates can be considered as a benzyloxycarbonyl (otherwise known as carbobenzyloxy, Cbz or Z) protecting group for amino groups. It was introduced as a versatile alternative to the ethoxy carbamate group in peptide synthesis.
調製方法
製造方法Benzyl carbamate is prepared by reacting benzyl chloroformate with ammonia. Benzyl chloroformate was slowly added to 5 times the volume of cold ammonia water (relative density 0.90) under vigorous stirring, the reaction mixture was placed at room temperature for 30 minutes, the precipitate was filtered out, washed with water and dried to obtain the finished product of benzyl carbamate.
純化方法If it smells of NH3, then dry it in a vacuum desiccator and recrystallise it from 2 volumes of toluene and dry it in a vacuum desiccator again. It forms glistening plates from toluene, and can be recrystallised from H2O [Martell & Herbst J Org Chem 6 878 1941, Carter et al. Org Synth Coll Vol III 168 1955]. [Beilstein 6 IV 2278.]
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