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RuCl2[(S)-(DM-BINAP)][(S)-DAIPEN]_分子结构_CAS_220114-01-2)
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RuCl2[(S)-(DM-BINAP)][(S)-DAIPEN]

产品号 693227 公司名称 Sigma Aldrich
CAS号 220114-01-2 公司网站 http://www.sigmaaldrich.com
分子式 C71H72Cl2N2O2P2Ru 电 话 1-800-521-8956
分子量 1219.267102 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 141013

产品价格信息

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产品别名

标题
RuCl2[(S)-(DM-BINAP)][(S)-DAIPEN]
IUPAC标准名
(4S)-1,1-dichloro-12',12',14',14'-tetrakis(3,5-dimethylphenyl)-3,3-bis(4-methoxyphenyl)-4-(propan-2-yl)-2,5-diaza-12'λ5,14'λ5-diphospha-1-ruthenaspiro[cyclopentane-1,13'-pentacyclo[13.8.0.02,11.03,8.018,23]tricosane]-1'(15'),2',4',6',8',10',16',18',20',22'-decaene
IUPAC传统名
(4S)-1,1-dichloro-12',12',14',14'-tetrakis(3,5-dimethylphenyl)-4-isopropyl-3,3-bis(4-methoxyphenyl)-2,5-diaza-12'λ5,14'λ5-diphospha-1-ruthenaspiro[cyclopentane-1,13'-pentacyclo[13.8.0.02,11.03,8.018,23]tricosane]-1'(15'),2',4',6',8',10',16',18',20',22'-decaene
别名
Dichloro[(S)-(-)-2,2′-bis[di(3,5-xylyl)phosphino]-1,1′-binaphthyl][(2S)-(+)-1,1-bis(4-methoxyphenyl)-3-methyl-1,2-butanediamine]ruthenium(II)
二氯[(S)-(-)-2,2′-二[二(3,5-二甲苯基)膦基]-1,1′-联萘基][(2S)-(+)-1,1-二(4-甲氧苯基)-3-甲基-1,2-丁二胺]钌(II)

产品登记号

CAS号 220114-01-2

产品性质

Empirical Formula (Hill Notation) C71H74Cl2N2O2P2Ru
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26
保存温度 2-8°C
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
50, 100 mg in glass bottle
Legal Information
Sold in collaboration with Takasago for research purposes only. JP Registration No. 2041996, 2731377, 2935453 JP Appllication No. 19970359654
Application
Takasago Ligands and Complexes for Asymmetric Reactions
Catalyst for:
• Preparation of cyclometalated ruthenium 1,1-dianisyl-2-isopropyl-1,2-ethylenediamine complexes via asymmetric hydrogenation of ketones
• Enantioselective hydrogenation of an α-alkoxy substituted ketone with chiral ruthenium (phosphinoferrocenyl)oxazoline complexes
• Nonclassical asymmeteric hydrogen transfer between alcohols and carbonyl compounds
• Asymmetric hydrogenation of amino and heteroaromatic ketones
• Pharmacologically active substituted oxazolidinone used as NPC1L1 ligand for inhibition of cholesterol absorption
详细说明 (简体中文)
包装
50, 100 mg in glass bottle
Legal Information
与 Takasago 合作销售,仅用于研究目的。日本注册号 041996, 2731377, 2935453,日本申请号19970359654
Application
Takasago Ligands and Complexes for Asymmetric Reactions
Catalyst for:
• Preparation of cyclometalated ruthenium 1,1-dianisyl-2-isopropyl-1,2-ethylenediamine complexes via asymmetric hydrogenation of ketones
• Enantioselective hydrogenation of an α-alkoxy substituted ketone with chiral ruthenium (phosphinoferrocenyl)oxazoline complexes
• Nonclassical asymmeteric hydrogen transfer between alcohols and carbonyl compounds
• Asymmetric hydrogenation of amino and heteroaromatic ketones
• Pharmacologically active substituted oxazolidinone used as NPC1L1 ligand for inhibition of cholesterol absorption

参考文献