2-ブロモ-5-メトキシベンゾニトリル

2-Bromo-5-methoxybenzonitrile

HCID 21784096CAS 138642-47-4

基本情報

標準SMILES
COc1ccc(Br)c(C#N)c1
InChIKey
ZQONVYONOASKIY-UHFFFAOYSA-N
分子式
C8H6BrNO
平均分子量
212.04 g/mol
単同位体質量
210.96327591

名称と識別子

優先名称
2-Bromo-5-methoxybenzonitrile
IUPAC
2-bromo-5-methoxybenzonitrile
現地名
2-ブロモ-5-メトキシベンゾニトリル
英語名
2-Bromo-5-methoxybenzonitrile
分子式
C8H6BrNO
分子量
212.04

名称と別名

2-bromo-5-methoxybenzonitrile138642-47-4DTXSID80617998RefChem:257370DTXCID60568752625-739-14-Bromo-3-cyanoanisoleMFCD01861260Benzonitrile, 2-bromo-5-methoxy-2-bromo-5-methoxybenzenecarbonitrile2-bromo-5-methoxy-benzonitrileSCHEMBL2038941
名称をさらに表示
2-ブロモ-5-メトキシベンゾニトリルKML-452-BroMo-5-Methoxybenzonitrile 97%4-Bromo-3-cyanoanisole, 6-Bromo-m-anisonitrile
SBB0287762-Bromo-5-methoxybenzonitrile, 97%AKOS000304719FB55427PS-3910AC-26258SY030656DB-027531

データベース識別子

CAS
138642-47-4
PubChem CID
21784096
DTXSID
DTXSID80617998
EC Number
625-739-1
Nikkaji
J3.182.828G

物性

構造計算による物性

XLogP
2.3
極性表面積
33 Ų
水素結合供与体数
0
水素結合受容体数
2
回転可能結合数
1
重原子数
11

物理化学的性質

融点
99 · 99-102 °C
沸点
292.8 · 292.8±30.0 °C(Predicted)
比重(密度)
1.56 · 1.56±0.1 g/cm3(Predicted)
貯蔵温度
2 · 2-8°C
外見
solid
色
peachy

安全と法規制

GHS分類

GHS Classification · 4 件

Warning

H302 (97.8%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, 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 46 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Hazard Classes and CategoriesAcute Tox. 4 (97.8%)

安全データ

wgk
3
ridadr
UN3439
hs_code
29269090
risk_code
22
hazard_code
Xn
safety_code
36/37

化学と産業

応用分野 · 1 件

使用2-Bromo-5-methoxybenzonitrile (10.0 g, 47.2 mmol) was dissolved in dry tetrahydrofuran (100 mL) in a flame-dried flask and cooled in an ice bath. A solution of borane in tetrahydrofuran (75 mL, 75 mmol, 1.0 M) was added dropwise over 30 minutes. The reaction mixture was stirred overnight at rt, then quenched slowly with ice water and Na2CO3 (saturated aqueous solution). After removing THF, the residue was extracted with large amounts of EtOAc three times. The combined organic layers were washed with water, dried, and concentrated to give the crude, which was purified by silica gel column chromatography to give 1-(2-Bromo-5-methoxyphenyl)methanamine as a white powder (3.65 g, 36%).

サプライヤー50 社

苏州道澜生物医药科技有限公司15952404857 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
上海凌富药物研究有限公司+86(21)5895 0110 19945755304 · [email protected]
Hebei Chuanghai Biotechnology Co., Ltd+86-17732866630 · [email protected]
上海策嵘生物科技有限公司[email protected]

関連反応

6 件

関連ノート

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