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Benzonitrile, 2-nitro-6-(phenylmethoxy)-, also known as 2-Nitro-6-(phenylmethoxy)benzonitrile, is an organic compound with the chemical formula C13H10N2O3. It is a derivative of benzonitrile, featuring a nitro group at the 2-position and a phenylmethoxy group at the 6-position. Benzonitrile, 2-nitro-6-(phenylmethoxy)- is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used in the synthesis of pharmaceuticals and other organic compounds due to its unique chemical structure and reactivity. The compound's properties, such as its nitro and phenylmethoxy groups, make it a valuable intermediate in the development of various chemical products.

1591-33-9

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1591-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1591-33-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1591-33:
(6*1)+(5*5)+(4*9)+(3*1)+(2*3)+(1*3)=79
79 % 10 = 9
So 1591-33-9 is a valid CAS Registry Number.

1591-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-6-phenylmethoxybenzonitrile

1.2 Other means of identification

Product number -
Other names Benzonitrile,2-nitro-6-(phenylmethoxy)

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:1591-33-9 SDS

1591-33-9Relevant academic research and scientific papers

Antifolate and Antibacterial Activities of 5-Substituted 2,4-Diaminoquinazolines

Harris, Neil V.,Smith, Christopher,Bowden, Keith

, p. 434 - 444 (2007/10/02)

A series of 5-substituted 2,4-diaminoquinazolines (3) has been synthesized and evaluated as inhibitors of the enzyme dihydrofolate reductase (DHFR) from both bacterial and mammalian sources.The best compounds (e.g. 53) show good activity against Escherichia coli DHFR, but there is no significant selectivity for the bacterial over the mammalian enzyme.The structure-activity relationships for enzyme inhibition appear to be complex and not amenable to simple analysis; a hypotesis to explain the observed qualitative structure-activity relationships is proposed.The inhibitory activities of the compounds against the growth of intact bacterial cells in vitro closely parallel those for the inhibition of the isolated bacterial enzymes, suggesting that their antifolate action is responsible for their antibacterial effects.Five of the compounds were tested for their ability to cure a systemic E. coli infection in the mouse, but they showed no therapeutic effects at their maximum tolerated doses.

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