基本情報
- CAS
57489-77-7- 標準SMILES
Clc1cc(Cl)n2nccc2n1- InChIKey
JMTFWCYVZOFHLR-UHFFFAOYSA-N- 分子式
- C6H3Cl2N3
- 平均分子量
- 188.01 g/mol
- 単同位体質量
- 186.97040246
名称と識別子
- 優先名称
- 5,7-Dichloropyrazolo[1,5-a]pyrimidine
- IUPAC
- 5,7-dichloropyrazolo[1,5-a]pyrimidine
- 現地名
- 5,7-ジクロロピラゾロ[1,5-A]ピリミジン
- 英語名
- 5,7-Dichloropyrazolo[1,5-a]pyrimidine
- 分子式
- C6H3Cl2N3
- 分子量
- 188.01
名称と別名
名称をさらに表示
データベース識別子
- CAS
57489-77-7- PubChem CID
- 11074154
- DTXSID
DTXSID50454231- ChEMBL
CHEMBL3747320- EC Number
- 890-692-8
- Nikkaji
- J1.087.013E
物性
構造計算による物性
- XLogP
- 2.2
- 極性表面積
- 30.2 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
- 0
- 重原子数
- 11
- 形式電荷
- 0
- 複雑度
- 155
物理化学的性質
- 融点
- 68 · 68-71 °C(Solv: ethanol (64-17-5))
- 比重(密度)
- 1.69 · 1.69±0.1 g/cm3(Predicted)
- 貯蔵温度
- 2 · under inert gas (nitrogen or Argon) at 2–8 °C
- 酸解離定数(Pka)
- -1.68 · -1.68±0.30(Predicted)
- 外見
- Solid
- 色
- Off-white to yellow
- InChI
- InChI=1S/C6H3Cl2N3/c7-4-3-5(8)11-6(10-4)1-2-9-11/h1-3H
- InChIKey
- JMTFWCYVZOFHLR-UHFFFAOYSA-N
- SMILES
- C12=CC=NN1C(Cl)=CC(Cl)=N2
安全と法規制
GHS分類
GHS Classification
Danger
H301 (33.3%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P272, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P333+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 3 reports by companies from 3 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
- hs_code
- 2933599590
化学と産業
応用分野
使用5,7-Dichloropyrazolo[1,5-a]pyrimidine is a pharmaceutical intermediate compound that can be used in a palladium-catalysed pharmaceutical synthesis cross-coupling reaction. 2,4-Dichloroquinoline reacts with benzylzinc and phenylzinc reagents in the presence of catalytic quantities of palladium complexes to yield only α-substituted products.2,4-Dichloroquinolines have been found to react with benzylzinc and phenylzinc reagents in catalytic amounts of palladium compounds to produce only α-substituted products. LiCl was found to be an effective additive for γ-selective coupling reactions. These α- or γ-selective coupling conditions are applicable to the reaction of 5,7-Dichloropyrazolo[1,5-a]pyrimidine and biphenylmethyl zinc reagents in the synthesis of angiotensin II receptor antagonists. This regioselectivity should be generally applicable to other α,γ-dichloropyrazine systems[1].
上流・下流製品情報
上流原料
下流製品
サプライヤー100 社
関連反応
化合物ノート
読み込み中…