产品名称

英文名称：1,1′-Binaphthyl-2,2′-diamine

同义词

4488-22-6、[1,1'-Binaphthalene]-2,2'-diamine、18531-95-8、18741-85-0、1,1'-Binaphthyl-2,2'-diamine、(R)-[1,1'-Binaphthalene]-2,2'-diamine、(S)-(-)-1,1'-Binaphthyl-2,2'-diamine、(R)-(+)-2,2'-Diamino-1,1'-binaphthalene、(S)-(-)-2,2'-Diamino-1,1'-binaphthalene、2,2'-、( )-1,1'-双(2-萘胺)、1,1'-联萘-2,2'-二胺、2,2'-二氨基-1,1'-联萘

产品性质

CAS编号：4488-22-6

分子式：C20H16N2

分子量：284.35

MDL号：MFCD00145204

PubChem编号：20571

别名：( )-1,1'-双(2-萘胺)|1,1'-联萘-2,2'-二胺|2,2'-二氨基-1,1'-联萘

英文别名：4488-22-6|[1,1'-Binaphthalene]-2,2'-diamine|18531-95-8|18741-85-0|1,1'-Binaphthyl-2,2'-diamine|(R)-[1,1'-Binaphthalene]-2,2'-diamine|(S)-(-)-1,1'-Binaphthyl-2,2'-diamine|(R)-(+)-2,2'-Diamino-1,1'-binaphthalene|(S)-(-)-2,2'-Diamino-1,1'-binaphthalene|2,2'-

规格或纯度：97%

英文名称：1,1′-Binaphthyl-2,2′-diamine

运输条件：常规运输

产品介绍：ApplicationNovel axially chiral Rh N-heterocyclic carbene complexes were prepared from axially dissymmetric 1,1'-binaphthalenyl-2,2'-diamine and applied in the Rh-catalyzed enantioselective hydrosilylation of methyl ketones. The enantioselective direct aldol reaction, organocatalyzed by recoverable BINAM- prolinamide derivatives can be highly accelerated by a catalytic amount of a carboxylic acid without a detrimental of the obtained enantioselectivities.

IUPAC Name：1-(2-aminonaphthalen-1-yl)naphthalen-2-amine

INCHI：InChI=1S/C20H16N2/c21-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)22/h1-12H,21-22H2

InChi Key：DDAPSNKEOHDLKB-UHFFFAOYSA-N

Canonical SMILES：C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)N)N

Isomeric SMILES：C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)N)N

WGK Germany：3

RTECS：DU3090000

PubChem CID：20571

Reaxy-Rn：2138401

溶解性：Insoluble in water

熔点：188-193°C

象形图：

信号词：Danger

危险声明：H302 Harmful if swallowedH318 Causes serious eye damage

预防措施声明：P280,P501,P264,P270,P330,P264+P265,P301+P317,P305+P354+P338,P317

个人防护装备：dust mask type N95 (US), Eyeshields, Gloves

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