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N-(3,5-dimethoxy-2-nitrophenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1075748-42-3 Structure
  • Basic information

    1. Product Name: N-(3,5-dimethoxy-2-nitrophenyl)acetamide
    2. Synonyms: N-(3,5-dimethoxy-2-nitrophenyl)acetamide
    3. CAS NO:1075748-42-3
    4. Molecular Formula:
    5. Molecular Weight: 240.216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1075748-42-3.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: N-(3,5-dimethoxy-2-nitrophenyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3,5-dimethoxy-2-nitrophenyl)acetamide(1075748-42-3)
    11. EPA Substance Registry System: N-(3,5-dimethoxy-2-nitrophenyl)acetamide(1075748-42-3)
  • 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: 1075748-42-3(Hazardous Substances Data)

1075748-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1075748-42-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,5,7,4 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1075748-42:
(9*1)+(8*0)+(7*7)+(6*5)+(5*7)+(4*4)+(3*8)+(2*4)+(1*2)=173
173 % 10 = 3
So 1075748-42-3 is a valid CAS Registry Number.

1075748-42-3Downstream Products

1075748-42-3Relevant articles and documents

Substituent effects in solid-state assembly of activated benzotriazoles

Wenholz, Daniel S.,Bhadbhade, Mohan,Kandemir, Hakan,Ho, Junming,Kumar, Naresh,Black, David Stc.

, p. 835 - 842 (2019)

Aromatic donor-acceptor stacking involving electron-rich π-donors and electron-deficient π-acceptors has been utilized in a broad spectrum of diverse applications to great effect. We report the discovery of unprecedented donor-acceptor stacking from a non

Synthesis of dimethoxy activated benzimidazoles and bisbenzimidazoles

Alamgir, Mahiuddin,Black, David St C.,Bowyer, Paul K.,Condie, Glenn C.,Kumar, Naresh,Martinovic, Vesna,Sholihin, Hayat,Wood, Joanne

, p. 1189 - 1217 (2020/09/18)

A range of 2-substituted-4,6-dimethoxy activated benzimidazoles and 2,2'-bisbenzimidazoles have been synthesized from 2-aminoanilide derivatives under acidic conditions. The starting materials were prepared either by acylation from 3,5-dimethoxyaniline followed by nitration, or by acylation from 3,5-dimethoxy-2-nitroaniline. The 2-nitroanilides were then reduced by palladium catalyzed reaction with hydrazine and subsequent acid catalyzed cyclization giving the corresponding 4,6-dimethoxybenzimidazoles and 4,6-dimethoxy-2,2'-bisbenzimidazoles. In addition, 2-phenyl-4,5,6-trimethoxybenzimidazole has been synthesized using a similar procedure.

Regioselective nitration of anilines with Fe(NO3)3·9H2O as a promoter and a nitro source

Gao, Yang,Mao, Yuanyou,Zhang, Biwei,Zhan, Yingying,Huo, Yanping

, p. 3881 - 3884 (2018/06/08)

An efficient Fe(NO3)3·9H2O promoted ortho-nitration reaction of aniline derivatives has been developed. This reaction may go through a nitrogen dioxide radical (NO2) intermediate, which is generated by the thermal decomposition of iron(iii) nitrate. The practicality of the present method using nontoxic and inexpensive iron reagents has been shown by the broad substrate scope and applications.

Regioselective ortho-nitration of N-phenyl carboxamides and primary anilines using bismuth nitrate/acetic anhydride

Lu, Yang,Li, Yaming,Zhang, Rong,Jin, Kun,Duan, Chunying

supporting information, p. 9422 - 9427 (2013/10/08)

An efficient and one-pot synthetic method for the regioselective ortho-nitration of the N-phenyl carboxamides and primary anilines has been developed by using bismuth nitrate and acetic anhydride as the nitrating reagents. Reaction proceeds at room temperature and results in corresponding ortho-nitrated products in moderate to excellent yields. This method provides an operationally simple, regioselective, and efficient access to synthesize o-nitro anilines under the mild conditions.

BRIDGED SIX-MEMBERED RING COMPOUNDS

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Page/Page column 94, (2008/12/08)

The invention relates to compounds of formula (I), wherein R1, R2, R1a, R2a, R3, R4, A, B, X, W and n are as defined in the description, and pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium channel blockers.

Imidazoquinoxaline protein tyrosine kinase inhibitors

-

, (2008/06/13)

Novel imidazoquinoxalines and salts thereof, pharmaceutical compositions containing such compounds, and methods of using such compounds in the treatment of protein tyrosine kinase-associated disorders such as immunologic disorders.

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