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1823-15-0

4-(3-Nitro-phenyl)-buttersaeure, also known as 4-(3-nitrophenyl)butanoic acid, is an organic compound with the chemical formula C10H11NO4. It is a derivative of butyric acid, featuring a nitro group attached to the phenyl ring at the 3-position and a butanoic acid chain at the 4-position. This yellow crystalline solid is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Its chemical structure and properties make it a versatile building block in the development of new compounds with specific biological activities.

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  • 1823-15-0 Structure

  • Basic information

    1. Product Name: 4-(3-Nitro-phenyl)-buttersaeure
    2. Synonyms: 4-(3-Nitro-phenyl)-buttersaeure
    3. CAS NO:1823-15-0
    4. Molecular Formula:
    5. Molecular Weight: 209.202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1823-15-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(3-Nitro-phenyl)-buttersaeure(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(3-Nitro-phenyl)-buttersaeure(1823-15-0)
    11. EPA Substance Registry System: 4-(3-Nitro-phenyl)-buttersaeure(1823-15-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1823-15-0(Hazardous Substances Data)

1823-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1823-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1823-15:
(6*1)+(5*8)+(4*2)+(3*3)+(2*1)+(1*5)=70
70 % 10 = 0
So 1823-15-0 is a valid CAS Registry Number.

1823-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-Nitro-phenyl)-buttersaeure

1.2 Other means of identification

Product number -
Other names -

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:1823-15-0 SDS

1823-15-0Upstream product

1823-15-0Downstream Products

1823-15-0Relevant articles and documents

Experiments on the Chaperon effect in the nitration of aromatics

Strazzolini, Paolo,Giumanini, Angelo G.,Runcio, Antonio,Scuccato, Massimo

, p. 952 - 958 (2007/10/03)

A nitro group may be effectively delivered to the ortho position of alkylbenzenes, provided that a suitable chaperon function is located in α- position and a dilute of HNO3 in CH2Cl2 is used. The carbonyl function of an aldehyde or ketone is the best choice, but a carboxyl, alkoxycarbonyl, and amide groups all work well. The ether function showed a less pronounced ortho orientation effect, whereas the hydroxyl group was too prone to oxidation. Side reactions were minimal under the conditions employed. A para chaperon effect was seemingly at work in the CH2Cl2 nitration of benzenepropanenitrile. All the results were compared with the corresponding classical nitration in H2SO4.

Polyiodinated triglyceride analogs as potential computed tomography imaging agents for the liver

Weichert,Longino,Bakan,Spigarelli,Chou -,Schwendner,Counsell

, p. 636 - 646 (2007/10/02)

A series of glyceryl 2-oleoyl 1,3-bis[ω-(3-amino-2,4,6-triiodophenyl)] alkanoates was synthesized, radioiodinated with iodine-125, emulsified, and evaluated for their ability to selectively localize in the liver for potential use as hepatographic agents i

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