4'-ブロモアセトアニリド

4'-Bromoacetanilide

HCID 7683CAS 103-88-8

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

4'-Bromoacetanilide103-88-84-BROMOACETANILIDEN-(4-Bromophenyl)acetamidep-BromoacetanilideBromoanilideAcetamide, N-(4-bromophenyl)-BromoantifebrinAntisepsinAsepsinN-Acetyl-4-bromoanilinep-Bromo-N-acetanilide
名称をさらに表示
4'-ブロモアセトアニリドアンチセプシンブロモアニリドN-(4-ブロモフェニル)アセトアミドブロモアンチフェブリンN-アセチル-4-ブロモアニリンN-(p-ブロモフェニル)アセトアミド4-ブロモ-1-アセチルアミノベンゼンアセプシン1-ブロモ-4-(アセチルアミノ)ベンゼンp-ブロモアセトアニリド4′-ブロモアセトアニリド4′‐ブロモアセトアニリド4-ブロモアセトアニリド4'-ブロモアセトアニリド, 98%Bromoacetanilide4-BROMOACETOANILIDE4-Bromoacetanilide, 98% PSusafdo-40Bromanilide
1-Bromo-4-acetamidobenzeneAcetanilide, p-bromo-USAF DO-40Acetanilide, 4'-bromo-N-(4-Bromo-phenyl)-acetamideN-Acetyl-p-bromoanilineNSC 105442N-(p-Bromophenyl)acetamide

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

実験および物理化学的性質

SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP2.14

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
化学的性質 · 1 件

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 · 4 件

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 · 2 件

Chemical: Acetamide, N-(4-bromophenyl)-

Acetamide, N-(4-bromophenyl)-: Does not have an individual approval but may be used under an appropriate group standard

Hazard Classes and CategoriesSkin Irrit. 2 (97.9%)

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

化学と産業

用途と製造

General Manufacturing InformationAcetamide, N-(4-bromophenyl)-: ACTIVE
応用分野 · 1 件

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 · 2 件

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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