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5111-70-6

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5111-70-6 Usage

Chemical Properties

white to light yellow crystal powder

Synthesis Reference(s)

Journal of the American Chemical Society, 106, p. 2469, 1984 DOI: 10.1021/ja00320a060The Journal of Organic Chemistry, 35, p. 647, 1970 DOI: 10.1021/jo00828a022Tetrahedron Letters, 8, p. 2763, 1967

General Description

The cytotoxic potential of 5-methoxy-1-indanone was assessed.

Check Digit Verification of cas no

The CAS Registry Mumber 5111-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5111-70:
(6*5)+(5*1)+(4*1)+(3*1)+(2*7)+(1*0)=56
56 % 10 = 6
So 5111-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-12-8-3-4-9-7(6-8)2-5-10(9)11/h3-4,6H,2,5H2,1H3

5111-70-6 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (L11165)  5-Methoxy-1-indanone, 98%   

  • 5111-70-6

  • 1g

  • 311.0CNY

  • Detail
  • Alfa Aesar

  • (L11165)  5-Methoxy-1-indanone, 98%   

  • 5111-70-6

  • 5g

  • 1010.0CNY

  • Detail

5111-70-6SDS

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 5-Methoxy-1-indanone

1.2 Other means of identification

Product number -
Other names 1H-Inden-1-one, 2,3-dihydro-5-methoxy-

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:5111-70-6 SDS

5111-70-6Relevant articles and documents

Facile transformation of benzocyclobutenones into 2,3-benzodiazepines via 4π-8π tandem electrocyclic reactions involving net insertion of diazomethylene compounds

Matsuya, Yuji,Ohsawa, Noriko,Nemoto, Hideo

, p. 13072 - 13073 (2006)

Efficient transformations of benzocyclobutenones into 2,3-benzodiazepines by a formal insertion of diazomethylene compounds are described. This sequential process includes nucleophilic addition of diazomethylene anion, oxy-anion accelerated o-quinodimethane formation by an electrocyclic ring-opening reaction, and 8π-electrocyclization in one-pot under remarkably mild conditions. Intermediary oxy-anion plays an important role for the efficient transformations. Copyright

Electrochemical Difunctionalization of Styrenes via Chemoselective Oxo-Azidation or Oxo-Hydroxyphthalimidation

Jiang, Haobin,Wang, Feng,Ye, Zenghui,Zhang, Fengzhi,Zhu, Rongjin

supporting information, p. 8240 - 8245 (2021/11/17)

Atom- and step-economic oxo-azidation and oxo-hydroxyphthalimidation of styrenes have been developed under mild electrolytic conditions, respectively. Various valuable alpha-azido or hydroxyphthalimide aromatic ketones were synthesized efficiently from readily available styrenes, azides, and N-hydroxyphthalimides. Mechanism studies show that two different pathways involved in these two transformations.

BENZOCYCLOOCTENE-BASED AND INDENE-BASED ANTICANCER AGENTS

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Paragraph 0095, (2018/02/27)

Benzocyclooctene (fused 6,8 ring system) analogues and corresponding indene (fused 6,5 ring system) analogues function as inhibitors of tubulin polymerization. The compounds are useful as anticancer agents in a new therapeutic approach for cancer treatment utilizing small-molecule inhibitors of tubulin polymerization that also act as vascular disrupting agents (VDAs).

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