基本情報
- 標準SMILES
CC(=O)Nc1ccc(Br)cc1- InChIKey
MSLICLMCQYQNPK-UHFFFAOYSA-N- 分子式
- C8H8BrNO
- 平均分子量
- 214.06 g/mol
- 単同位体質量
- 212.97892598
名称と識別子
- 優先名称
- 4'-Bromoacetanilide
- IUPAC
- N-(4-bromophenyl)acetamide
- 現地名
- 4'-ブロモアセトアニリド
- 英語名
- 4'-Bromoacetanilide
- 分子式
- C8H8BrNO
- 分子量
- 214.06
名称と別名
名称をさらに表示
データベース識別子
- CAS
103-88-8- PubChem CID
- 7683
- DTXSID
DTXSID6059283- ChEMBL
CHEMBL59019- UNII
- 4KB44F25A3
- EC Number
- 203-154-9
- Nikkaji
- J37.694I
物性
構造計算による物性
- XLogP
- 2.3
- 極性表面積
- 29.1 Ų
- 水素結合供与体数
- 1
- 水素結合受容体数
- 1
- 回転可能結合数
- 1
- 重原子数
- 11
- 形式電荷
- 0
- 複雑度
- 141
実験および物理化学的性質
物理化学的性質
- 融点
- 165 · 165-169 °C(lit.)
- 沸点
- 353.4 °C · 353.4°C (estimate)
- 比重(密度)
- 1.72 · 1.72
- 屈折率
- 1.612 · 1.6120 (estimate)
- 貯蔵温度
- 30 °C · Store below +30°C.
- 溶解性
- アルコール:適度に溶ける
- 外見
- 結晶性粉末または結晶
- 酸解離定数(Pka)
- 14.25 · 14.25±0.70(Predicted)
- 色
- ホワイトからベージュまたはライトグレー
- 水溶解度
- 不溶性
- Merck
- 14 · 14,1399
- BRN
- 2208091 · 2208091
- 安定性
- 安定。強力な酸化剤とは相容れない。
- InChI
- 1S/C8H8BrNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)
- InChIKey
- MSLICLMCQYQNPK-UHFFFAOYSA-N
- SMILES
- CC(=O)Nc1ccc(Br)cc1
- CAS データベース
- 103 · 103-88-8(CAS DataBase Reference)
- NISTの化学物質情報
- Acetamide, N-(4-bromophenyl)-(103-88-8)
- EPAの化学物質情報
- Acetamide, N-(4-bromophenyl)- (103-88-8)
化学的性質
化学的特性4'-Bromoacetanilide is a white to light beige crystalline solid with a melting point of 168°C and a relative density of 1.717. It is soluble in benzene, chloroform, and ethyl acetate, slightly soluble in alcohol and hot water, and insoluble in cold water. This compound can be prepared by brominating acetanilide and is commonly used as an intermediate in organic synthesis.
安全と法規制
GHS分類
GHS Classification
Warning
H315 (97.9%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 48 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
Chemical: Acetamide, N-(4-bromophenyl)-
Acetamide, N-(4-bromophenyl)-: Does not have an individual approval but may be used under an appropriate group standard
安全データ
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- AD9625000
- ridadr
- 2811
- 毒性
- mouse,LD50,intraperitoneal,250mg/kg (250mg/kg),National Technical Information Service. Vol. AD277-689,
- hs_code
- 29242998
- risk_code
- 36/37/38
- 化審法
- (3)-196
- hazard_code
- Xi
- hazard_note
- Irritant
- safety_code
- 26-36
- hazard_class
- 6.1(b)
- packing_group
- III
- ストレージクラス
- 11 - Combustible Solids
化学と産業
用途と製造
応用分野
使用4'-Bromoacetanilide is used as an internal standard for phenylurea and the respective metabolic products in oysters. It has also been used as a reagent in the production of a new ligand to form a coordination compex between gadolinium(III) and T=titanium(IV) oxide. It was used in the synthesis of new ligand for anchoring Gd(III) chelates onto TiO2 surface.
調製方法
製造方法Preparation of 4'-Bromoacetanilide from Acetanilide. Principle: Aromatic compounds can be conveniently brominated by the use of brominating agent, which is normally a solution of bromine in acetic acid. Bromination of activated aromatic compounds usually give 2, 4, 6-tribromo derivatives while moderately activating group like anilide give preferably the para bromo product. Reaction: Procedure: Dissolve 0.5 g acetanilide in 0.6 ml glacial acetic acid and add 2.5 ml bromine solution in acetic acid (25% w/v). Shake the mixture for 1 h. After 1 h, pour the mixture on to crushed ice (20 g) with stirring. Filter the separated product and wash with cold water. Dry the product, record the practical yield and re-crystallize it. Re-crystallization: Dissolve the crude product in minimum amount of ethyl alcohol in a beaker by heating on a water bath. Filter the hot solution and cool the filtrate. The crystals of the product separate out. Filter, dry and record the melting point and TLC (using toluene as a solvent).
純化方法Crystallise the anilide from aqueous MeOH or EtOH. Purify it by zone refining. [Beilstein 12 IV 1504.]
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