5,7-ジクロロピラゾロ[1,5-A]ピリミジン

5,7-Dichloropyrazolo[1,5-a]pyrimidine

HCID 11074154

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

5,7-Dichloropyrazolo[1,5-a]pyrimidine57489-77-75,7-dichloropyrazolo(1,5-a)pyrimidineDTXSID50454231RefChem:298820DTXCID40405050890-692-8MFCD08273918PYRAZOLO[1,5-A]PYRIMIDINE, 5,7-DICHLORO-SCHEMBL29869CHEMBL3747320BDBM50500533
名称をさらに表示
5,7-ジクロロピラゾロ[1,5-A]ピリミジンoropyrazoLo[1,5-a]pyrimidine7-dichloropyrazolo[15,7-DICHLOROPYRAZOLO[1,5-A]PYRIMIDINE CAS 57489-77-7
AKOS006286728CS-W003486GS-65925,7-Dichloro-pyrazolo[1,5-a]pyrimidineBCP100315,7-DichAM20100408FT-0650393

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

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

安全と法規制

GHS分類

GHS Classification · 4 件

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

Hazard Classes and CategoriesAcute Tox. 3 (33.3%)

安全データ

hs_code
2933599590

化学と産業

応用分野 · 1 件

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].

サプライヤー100 社

温州共赢化学有限公司+86-0086-577-64498589 +86-15355981851 · [email protected]
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]
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関連反応

39 件

化合物ノート

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