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内消旋-1,2-二苯基乙二胺

内消旋-1,2-二苯基乙二胺名称

[ CAS 号 ]:
951-87-1

[ 中文名 ]:
meso-1,2-二苯基乙烯基二胺

[ 英文名 ]:
meso-1,2-Diphenylethylenediamine

[中文别名 ]:

1,2-二苯基乙二胺

[英文别名 ]:

(1R,2R)-(+)-1,2-Diphenyl-1,2-ethanediamine
meso-1,2-Diphenylethylenediamine
(1R,2R)-(+)-1,2-Diphenylethylenediamine
(1R,2S)-1,2-Diphenyl-1,2-ethanediamine
(1R,2R)-1,2-Diphenylethan-1,2-diamin
(1R,2R)-1,2-Diphenylethylenediamine
(1R,2R)-(+)-1,2-Diamino-1,2-diphenylethane
(1R,2S)-1,2-diphenylethane-1,2-diamine
CH06110 MESO-1,2-DIPHENYLETHYLENEDIAMINE
(1R,2R)-1,2-Diphenyl-1,2-ethanediamine

内消旋-1,2-二苯基乙二胺物理化学性质

[ 密度 ]:
1.106g/cm3

[ 沸点 ]:
353.9ºC at 760mmHg

[ 熔点 ]:
118-122ºC

[ 分子式 ]:
C₁₄H₁₆N₂

[ 分子量 ]:
212.29000

[ 闪点 ]:
199.9ºC

[ 精确质量 ]:
212.13100

[ PSA ]:
52.04000

[ LogP ]:
3.78700

[ 外观性状 ]:
固体;White to Yellow to Orange powder to crystal

[ 折射率 ]:
1.619

[ 储存条件 ]:
存放于惰性气体之中;避免空气

内消旋-1,2-二苯基乙二胺MSDS

内消旋-1,2-二苯基乙二胺安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

[ 危险品运输编码 ]:
NONH for all modes of transport

[ 海关编码 ]:
2921590090

内消旋-1,2-二苯基乙二胺合成路线

内消旋-1,2-二苯基乙二胺上下游产品

内消旋-1,2-二苯基乙二胺上游产品

内消旋-1,2-二苯基乙二胺下游产品

内消旋-1,2-二苯基乙二胺海关

[ 海关编码 ]: 2921590090

[ 中文概述 ]:
2921590090. 其他芳香多胺及衍生物及它们的盐. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

内消旋-1,2-二苯基乙二胺文献

Synthesis and characterisation of nickel Schiff base complexes containing the meso-1,2-diphenylethylenediamine moiety: selective interactions with a tetramolecular DNA quadruplex.

Dalton Trans. 44(7) , 3136-50, (2015)

As part of a program of preparing metal complexes which exhibit unique affinities towards different DNA structures, we have synthesised the novel Schiff base complex N,N'-bis-4-(hydroxysalicylidine)me...

Enantioseparation of 1-arylethanols via a supramolecular chiral host consisting of N-(2-naphthoyl)-L-aspartic acid and an achiral diamine.

Org. Biomol. Chem. 10(9) , 1877-82, (2012)

A supramolecular chiral host consisting of N-(2-naphthoyl)-L-aspartic acid (L-1) and meso-1,2-diphenylethylenediamine (2) is effective in enantioseparation of 1-arylethanols (up to 96% ee with 100% in...

Synthesis and antiviral activities of N-mono- and/or N,N'-di-carbamoyl and acyl derivatives of symmetrical diamines.

Chem. Pharm. Bull. 56(7) , 1052-8, (2008)

N-carbamoyl and N-acyl diamine derivatives were synthesized from symmetrical diamines by their addition to iso(thio)cyanates, cleavage reaction of acid anhydride, or N-acylation by acyl chloride. (1R,...

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