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2207-68-3

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2207-68-3 Usage

Chemical Properties

white to light yellow crystal powde

Uses

Different sources of media describe the Uses of 2207-68-3 differently. You can refer to the following data:
1. 1-(4(Nitrophenyl)glycerol is a useful additive for controlling swarming of Proteus bacteria on culture media.
2. 1-(4-Nitrophenyl)glycerol inhibits the coordinately regulated activities of swarming behavior and virulence factor expression in Proteus mirabilis.

Check Digit Verification of cas no

The CAS Registry Mumber 2207-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2207-68:
(6*2)+(5*2)+(4*0)+(3*7)+(2*6)+(1*8)=63
63 % 10 = 3
So 2207-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO5/c11-5-8(12)6-15-9-3-1-7(2-4-9)10(13)14/h1-4,8,11-12H,5-6H2

2207-68-3 Well-known Company Product Price

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

  • (L19968)  1-(4-Nitrophenyl)glycerol, 99%   

  • 2207-68-3

  • 250mg

  • 795.0CNY

  • Detail
  • Alfa Aesar

  • (L19968)  1-(4-Nitrophenyl)glycerol, 99%   

  • 2207-68-3

  • 1g

  • 2408.0CNY

  • Detail
  • Alfa Aesar

  • (L19968)  1-(4-Nitrophenyl)glycerol, 99%   

  • 2207-68-3

  • 5g

  • 9632.0CNY

  • Detail

2207-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-nitrophenyl)propane-1,2,3-triol

1.2 Other means of identification

Product number -
Other names 1-(4-Nitrophenyl)glycerol

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:2207-68-3 SDS

2207-68-3Relevant articles and documents

Tandem Benzylic Oxidation/Dihydroxylation of α-Vinyl- and α-Alkenylbenzyl Alcohols

Fernandes, Rodney A.,Kattanguru, Pullaiah

, p. 92 - 107 (2015/10/19)

A de novo tandem benzylic oxidative dihydroxylation of α-vinyl- and α-alkenylbenzyl alcohols has been developed to give α,β-dihydroxypropiophenones (=2,3-dihydroxy-1-phenylpropan-1-ones) and α,β-dihydroxyalkyl phenones. This method was shown to be substrate-selective and specific for the oxidation of benzylic alcohols.

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