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58556-75-5

58556-75-5

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58556-75-5 Usage

Uses

It is an intermediate in dyestuffs and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 58556-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58556-75:
(7*5)+(6*8)+(5*5)+(4*5)+(3*6)+(2*7)+(1*5)=165
165 % 10 = 5
So 58556-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H6Br2/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/h1-6H

58556-75-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail

  • TCI America

  • (D3624)  2,7-Dibromonaphthalene  >98.0%(GC)

  • 58556-75-5

  • 5g

  • 1,190.00CNY

  • Detail

  • TCI America

  • (D3624)  2,7-Dibromonaphthalene  >98.0%(GC)

  • 58556-75-5

  • 25g

  • 3,690.00CNY

  • Detail

  • Alfa Aesar

  • (H56097)  2,7-Dibromonaphthalene, 99%   

  • 58556-75-5

  • 250mg

  • 293.0CNY

  • Detail

  • Alfa Aesar

  • (H56097)  2,7-Dibromonaphthalene, 99%   

  • 58556-75-5

  • 1g

  • 820.0CNY

  • Detail

  • Alfa Aesar

  • (H56097)  2,7-Dibromonaphthalene, 99%   

  • 58556-75-5

  • 5g

  • 3593.0CNY

  • Detail

58556-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-Dibromonaphthalene

1.2 Other means of identification

Product number -
Other names Naphthalene,2,7-dibromo

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:58556-75-5 SDS

58556-75-5Relevant articles and documents

Enantioselective α-Benzylation of Acyclic Esters Using π-Extended Electrophiles

Schwarz, Kevin J.,Yang, Chao,Fyfe, James W. B.,Snaddon, Thomas N.

supporting information, p. 12102 - 12105 (2018/09/11)

The first asymmetric cooperative Lewis base/palladium catalyzed benzylic alkylation of acyclic esters is reported. This reaction proceeds via stereodefined C1-ammonium enolate nucleophiles. Critical to its success was the identification of benzylic phosphate electrophiles, which were uniquely reactive. Alkylated products were obtained with very high levels of enantioselectivity, and this method has been applied toward the synthesis of the thrombin inhibitor DX-9065a.

The effect of substituents on the syn-anti conformer ratio in naphthyl-based imidazolinium salts and their corresponding N-heterocyclic carbenes

Gatti, Michele,Wu, Linglin,Drinkel, Emma,Gaggia, Fiona,Blumentritt, Sascha,Linden, Anthony,Dorta, Reto

experimental part, p. 176 - 198 (2011/06/18)

Eight new N-heterocyclic carbenes (NHCs) featuring substituted naphthyl side chains were synthesized. These molecules are present in solution as a stable mixture of anti and syn conformers. Through careful tuning of the substituents on position 2 and 2,7

Synthesis of a Helical Ferrocene

Katz, Thomas J.,Pesti, Jaan

, p. 346 - 347 (2007/10/02)

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