meso-1,2-bis(1-naphthyl)ethylenediamine | 117106-39-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: meso-1,2-bis(1-naphthyl)ethylenediamine
• 英文别名: meso-1,2-di(1-naphthyl)-1,2-diaminoethane；1,2-di(naphthalen-1-yl)ethane-1,2-diamine；1,2-Dinaphthalen-1-ylethane-1,2-diamine
• CAS: 117106-39-5
• 化学式: C₂₂H₂₀N₂
• 分子量: 312.414
• InChiKey: VVJVMUUCGDSHBT-UHFFFAOYSA-N

物化性质

• 熔点：
  174-177 °C
• 沸点：
  529.8±45.0 °C(Predicted)
• 密度：
  1.201±0.06 g/cm3(Predicted)
• 稳定性/保质期：
  遵照规定使用和储存，则不会分解。

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  24
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  52
• 氢给体数：
  2
• 氢受体数：
  2

安全信息

• 危险品标志：
  C
• 安全说明：
  S45
• 危险类别码：
  R34

SDS

Name:	Meso-1 2-bis(1-naphthyl)ethylenediamine 99% Material Safety Data Sheet
Synonym:
CAS:	117106-39-5

Section 1 - Chemical Product MSDS Name:Meso-1 2-bis(1-naphthyl)ethylenediamine 99% Material Safety Data Sheet
Synonym:

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Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS

CAS#	Chemical Name	content	EINECS#
117106-39-5	meso-1,2-Bis(1-naphthyl)ethylenediamin	99%	unlisted

Hazard Symbols: C
Risk Phrases: 34

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Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Causes burns.
Potential Health Effects
Eye:
Causes eye burns.
Skin:
Causes skin burns.
Ingestion:
Causes gastrointestinal tract burns.
Inhalation:
Causes chemical burns to the respiratory tract.
Chronic:
Not available.

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Section 4 - FIRST AID MEASURES
Eyes: Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid immediately.
Skin:
Get medical aid immediately. Immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion:
Do not induce vomiting. Get medical aid immediately.
Inhalation:
Get medical aid immediately. Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen.
Notes to Physician:
Treat symptomatically and supportively.

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Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear.
Extinguishing Media:
Use foam, dry chemical, or carbon dioxide.

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Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Vacuum or sweep up material and place into a suitable disposal container.

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Section 7 - HANDLING and STORAGE
Handling:
Do not breathe dust, vapor, mist, or gas. Do not get in eyes, on skin, or on clothing. Use only in a chemical fume hood.
Storage:
Store in a cool, dry place. Store in a tightly closed container.
Corrosives area. Store under nitrogen.

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Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 117106-39-5: Personal Protective Equipment Eyes: Not available.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

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Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Solid
Color: Not available.
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 177 - 178 deg C
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C22H20N2
Molecular Weight: 312.41

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Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures. Light sensitive.
Conditions to Avoid:
Incompatible materials, light.
Incompatibilities with Other Materials:
Strong oxidizing agents.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, carbon dioxide.
Hazardous Polymerization: Will not occur.

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Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 117106-39-5 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
meso-1,2-Bis(1-naphthyl)ethylenediamine - Not listed by ACGIH, IARC, or NTP.

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Section 12 - ECOLOGICAL INFORMATION

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Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

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Section 14 - TRANSPORT INFORMATION

IATA
Shipping Name: CORROSIVE SOLID, BASIC, ORGANIC, N.O.S.*
Hazard Class: 8
UN Number: 3263
Packing Group: III
IMO
Shipping Name: CORROSIVE SOLID, BASIC, ORGANIC, N.O.S.
Hazard Class: 8
UN Number: 3263
Packing Group: III
RID/ADR
Shipping Name: CORROSIVE SOLID, BASIC, ORGANIC, N.O.S.
Hazard Class: 8
UN Number: 3263
Packing group: III

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Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: C
Risk Phrases:
R 34 Causes burns.
Safety Phrases:
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 36/37/39 Wear suitable protective clothing, gloves
and eye/face protection.
S 45 In case of accident or if you feel unwell, seek
medical advice immediately (show the label where
possible).
WGK (Water Danger/Protection)
CAS# 117106-39-5: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 117106-39-5 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 117106-39-5 is not listed on the TSCA inventory.
It is for research and development use only.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  meso-1,2-bis(1-naphthyl)ethylenediamine 、 Sinomeninon 以 氯仿 为溶剂， 以65%的产率得到
  参考文献：
  名称：

  Sinomenine derivatives with embedment of nitrogen-containing heterocycles exhibiting potent TNF-αinhibitory activity

  摘要：

  本研究探讨了含有小型药物类氮杂环基团的盐酸缬草碱衍生物对肿瘤坏死因子-α（TNF-α）产生的抑制作用。发现几种具有氯苯基取代基的新型盐酸缬草碱衍生物展现出比天然盐酸缬草碱及其他衍生物更强的TNF-α抑制活性。

  DOI：

  10.1007/s11426-012-4588-8

文献信息

• Process for production of amines
  申请人：Terada Masahiro

  公开号：US20070142639A1

  公开（公告）日：2007-06-21

  A process for producing an amine which is characterized by reacting an imine with a nucleophilic compound (except a trialkylsilyl vinyl ether) in the presence of a phosphoric acid derivative represented by the formula (1): wherein A 1 represents a spacer; X 1 and X 2 represent each independently a divalent nonmetal atom or a divalent nonmetal atomic group; and Y 1 is oxygen or sulfur. The invention provides a process by which amines (particularly optically active amines) useful as intermediates of medicines, agricultural chemicals, or the like can be produced without special post-treatment in high yield at high optical purity; and phosphoric acid derivatives (particularly optically active phosphoric acid derivatives) useful in the production of the amines.

  一种生产胺的方法，其特征在于在式（1）所代表的磷酸衍生物存在下，将亚胺与一种亲核化合物（三烷基硅基乙烯醚除外）反应： 其中A1代表一个间隔物；X1和X2分别独立表示二价非金属原子或二价非金属原子团；Y1为氧或硫。该发明提供了一种方法，通过该方法，可以在高光学纯度下高产率地生产用作药品、农药等中间体的胺（特别是光学活性胺），而无需进行特殊的后处理；以及用于生产这些胺的磷酸衍生物（特别是光学活性磷酸衍生物）。
• Enantioselective Reductive Coupling of Imines Templated by Chiral Diboron
  作者：Mingkang Zhou、Kaidi Li、Dongping Chen、Ronghua Xu、Guangqing Xu、Wenjun Tang

  DOI：10.1021/jacs.0c04558

  日期：2020.6.10

  We herein report a general, practical, and highly efficient method for asymmetric synthesis of a wide range of chiral vicinal diamines via reductive coupling of imines templated by chiral diboron. The protocol features high enantioselectivity and stereospecificity, mild reaction conditions, simple operating procedures, use of readily available starting materials, and a broad substrate scope. The method

  我们在此报告了一种通用、实用且高效的方法，通过手性二硼模板化的亚胺的还原偶联不对称合成各种手性邻二胺。该协议具有高对映选择性和立体特异性、温和的反应条件、简单的操作程序、使用现成的起始材料和广泛的底物范围。该方法表明了启用二硼的 [3,3]-σ 重排的普遍性。
• DIPHENYL-DIHYDRO-IMIDAZOPYRIDINONES
  申请人：Dominique Romyr

  公开号：US20080255119A1

  公开（公告）日：2008-10-16

  and the pharmaceutically acceptable salts and esters thereof X, R 1 , R 2 , Y 1 and Y 2 are described herein inhibit the interaction of MDM2 protein with a p53-like peptide and hence have anti proliferative activity.

  在这里描述的X、R1、R2、Y1和Y2的药用盐和酯抑制MDM2蛋白与类p53肽的相互作用，因此具有抗增殖活性。
• Synthesis, structural characterization, electrochemical behavior and anticancer activity of gold(<scp>iii</scp>) complexes of <i>meso</i>-1,2-di(1-naphthyl)-1,2-diaminoethane and tetraphenylporphyrin
  作者：Muhammad Altaf、Saeed Ahmad、Abdel-Nasser Kawde、Nadeem Baig、Abdullah Alawad、Saleh Altuwaijri、Helen Stoeckli-Evans、Anvarhusein A. Isab

  DOI：10.1039/c6nj00692b

  日期：——

  cisplatin were evaluated on three human cancer cell lines, A549 (lung cancer cells), MCF7 (breast cancer cells) and HCT15 (colon cancer cells) using MTT assay. The results indicated that the prepared gold(III) complexes were more potent than cisplatin in inhibiting the growth of the selected cancer cells. The IC50 data revealed that complex 3 was the most effective antiproliferative agent.

  三种金（III）配合物，[Au（npen）Cl 2 ] Cl·2H 2 O（1），[Au（npen）2 ] Cl 3（2）和[Au（TPP）] Cl（3）（npen =内消旋-1,2-二（1-萘基）-1,2-二氨基乙烷，TPP =内消旋-tetraphenylporphyrin）已经被合成，并使用元素分析，IR和NMR光谱特征，和它们（之一1通过X射线）晶体学。1的结构由[Au（npen）Cl 2]复离子，一个氯离子和两个水分子。络合离子中的金原子采用扭曲的正方形平面几何形状。电化学研究了1和2与L-酪氨酸，谷胱甘肽和溶菌酶的相互作用。电化学测量表明，金（III）保持稳定，并且在与蛋白质相互作用时不发生还原。在体外复合物的细胞毒性特性，以及顺铂的是，使用MTT测定三种人癌细胞系，A549（肺癌细胞），MCF7（乳腺癌细胞）和HCT15（结肠癌细胞）进行评价。结果表明，所制备的金（Ⅲ））复合
• TRANSITION METAL COMPLEXES FOR ENANTIOSELECTIVE CATALYSIS OF CARBON-CARBON, CARBON-HETEROATOM, AND CARBON-HYDROGEN BOND FORMING REACTIONS
  申请人：THE TEXAS A&M UNIVERSITY SYSTEM

  公开号：US20150165429A1

  公开（公告）日：2015-06-18

  In some embodiments, the present disclosure pertains to a compound, comprising a transition metal complex having the formula Φ-[M(x,y)-L 1 (w,v)-L 2 (t,u)-L 3 ] p+ An − m Z − p — m . In an embodiment of the present disclosure Φ may be A. In another embodiment Φ may be Δ. In some embodiments of the present disclosure, M is a transition metal. In a related embodiment, p is an integer corresponding to the oxidation state of M. In some embodiments of the present disclosure, each of x, y, w, v, t, and u independently comprise R. In other embodiments, each of x, y, w, v, t, and u independently comprise S. In an embodiment of the present disclosure, each of L 1 , L 2 , and L 3 independently is a ligand comprising a substituted diamine. In some embodiments, An″ comprises a lipophilic anion, where m is from 1 to 3, and where Z − comprises an optional second anion.

  在某些实施例中，本公开涉及一种化合物，包括具有公式Φ-[M（x，y）-L1（w，v）-L2（t，u）-L3]p+An−mZ−p—m的过渡金属配合物。在本公开的某种实施例中，Φ可以是A。在另一种实施例中，Φ可以是Δ。在本公开的某些实施例中，M是一种过渡金属。在相关实施例中，p是与M的氧化态相对应的整数。在本公开的某些实施例中，x，y，w，v，t和u中的每个都独立地包括R。在其他实施例中，x，y，w，v，t和u中的每个都独立地包括S。在本公开的某种实施例中，L1、L2和L3中的每个都独立地是包含取代二胺的配体。在某些实施例中，An″包括一个亲脂性阴离子，其中m从1到3，而Z−包括一个可选的第二个阴离子。