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479-27-6

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479-27-6 Usage

Chemical Properties

Off white powder

Uses

Different sources of media describe the Uses of 479-27-6 differently. You can refer to the following data:
1. Lubricating-oil antioxidant, analytical reagent
2. 1,8-Diaminonaphthalene is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

Flammability and Explosibility

Nonflammable

Purification Methods

Crystallise 1,8-diaminonaphthalene from water or aqueous EtOH, and sublime it in a vacuum. The N,N'-dimethyl derivative [20734-56-9] has m 103-104o and pK2 5 5.61, the N,N,N'-trimethyl-derivative [20734-57-0] has m 29-30o and pK2 5 6.43. [Hodgson et al. J Chem Soc 202 1945, Beilstein 13 IV 344.]

Check Digit Verification of cas no

The CAS Registry Mumber 479-27-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 479-27:
(5*4)+(4*7)+(3*9)+(2*2)+(1*7)=86
86 % 10 = 6
So 479-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2/c11-8-5-1-3-7-4-2-6-9(12)10(7)8/h1-6H,11-12H2

479-27-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A15966)  1,8-Diaminonaphthalene, 97%   

  • 479-27-6

  • 50g

  • 301.0CNY

  • Detail
  • Alfa Aesar

  • (A15966)  1,8-Diaminonaphthalene, 97%   

  • 479-27-6

  • 250g

  • 1295.0CNY

  • Detail
  • Alfa Aesar

  • (A15966)  1,8-Diaminonaphthalene, 97%   

  • 479-27-6

  • 1000g

  • 4655.0CNY

  • Detail
  • Sigma

  • (33170)  1,8-Diaminonaphthalene  for fluorescence, ≥98.0% (HPLC/NT)

  • 479-27-6

  • 33170-25G-F

  • 427.05CNY

  • Detail
  • Sigma

  • (33170)  1,8-Diaminonaphthalene  for fluorescence, ≥98.0% (HPLC/NT)

  • 479-27-6

  • 33170-100G-F

  • 1,377.09CNY

  • Detail
  • Aldrich

  • (D21405)  1,8-Diaminonaphthalene  99%

  • 479-27-6

  • D21405-5G

  • 374.40CNY

  • Detail
  • Aldrich

  • (D21405)  1,8-Diaminonaphthalene  99%

  • 479-27-6

  • D21405-100G

  • 1,030.77CNY

  • Detail

479-27-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-Diaminonaphthalene

1.2 Other means of identification

Product number -
Other names naphthalene-1,8-diamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:479-27-6 SDS

479-27-6Relevant articles and documents

Preparation method of a plurality of (hetero) aromatic polyamines

-

Paragraph 0018-0021; 0051-0052; 0054, (2021/09/15)

The invention relates to the field of organic functional new material chemicals, and discloses a novel process technology for preparing a plurality of (hetero) aromatic polyamines through corresponding (hetero) aromatic polyfunctional hydroxamic acids (hydroxamic acid) before (re-arrangement). These (hetero) aromatic polyamines are well-known dyes and pigment and pharmaceutical pesticide-related fields of very wide range of critical fine chemical materials.

Activated carbon supported bimetallic catalysts with combined catalytic effects for aromatic nitro compounds hydrogenation under mild conditions

Huang, Lei,Lv, Yang,Wu, Shengtao,Liu, Pingle,Xiong, Wei,Hao, Fang,Luo, He'an

, p. 76 - 85 (2019/04/01)

Non-noble nickel catalysts have been widely studied and tried in hydrogenation, however the problem of nickel particle sintering is more and more common in high-loaded nickel catalysts. A series of highly dispersed bimetallic Ni-M/AC (M = Cu, Co, Fe or Zn) catalysts were prepared by incipient wetness impregnation methods and applied in 1-nitronaphthalene hydrogenation to 1-naphthylamine under mild reaction conditions. The prepared catalysts were characterized by XRD, BET, H2-TPR, TEM, HRTEM, HAADF-STEM, XPS, ICP, FT-IR and H2 chemisorption. The results show that the introduction of the metal promoter inhibits the sintering of the nickel and enhances the reducibility of the catalysts, leading to higher ratio of effective Ni° on the surface of the support, especially for Ni-Zn/AC sample. Moreover, the results of XPS indicate that the electron donating effect of Cu promoter increases surface electronic density of Ni, as a result, the electron-rich Ni might be produced because of the interfacial electronic effect, which favors the desorption and further impedes the hydrogenation of N-naphthylhydroxylamine. Ni-Zn/AC-350 with smaller nickel particles, better dispersion and larger content of effective Ni° presents the best catalytic performance in 1-nitronaphthalene hydrogenation to 1-naphthylamine under mild reaction conditions, it gives 100% conversion of 1-nitronaphthalene and 96.82% selectivity to 1-naphthylamine under 0.6 MPa and 90℃ for 5 h. Additionally, superior performances are also obtained in hydrogenation reactions of nitrobenzene, chloronitrobenzene, 1,5-dinitronaphthalene and 1,8-dinitronaphthalene over Ni-Zn/AC catalysts. With good hydrogenation activity the catalyst shows, the application prospect in industrial production of aromatic amine from aromatic nitro compounds has been becoming more and more extension.

A Co2B Mediated NaBH4 Reduction Protocol Applicable to a Selection of Functional Groups in Organic Synthesis

Lundevall, Frida Johanne,Elumalai, Vijayaragavan,Drageset, Audun,Totland, Christian,Bj?rsvik, Hans-René

supporting information, p. 3416 - 3425 (2018/07/29)

A high-yielding and high-rate reduction method that operates with alkenes, alkynes, azides, nitriles, and nitroarenes was developed and optimized. The method makes use of sodium borohydride reduction of CoSO4 under release of hydrogen along with the formation of Co2B as a nanoparticle material. The produced Co2B activates the various functional groups for hydride reduction. The protocol was proven to operate with an assortment of functional groups to provide good to excellent yields. Furthermore, the reduction method was successfully adapted, implemented, and developed for a continuous flow approach using the multi-jet oscillating disk (MJOD) flow reactor platform at atmospheric pressure.

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