Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(3-nitrophenyl)(pyrrolidin-1-yl)methanone is a chemical compound with the molecular formula C11H12N2O3. It is composed of a nitrophenyl group, a pyrrolidin-1-yl group, and a methanone group. (3-nitrophenyl)(pyrrolidin-1-yl)methanone is commonly known as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and it may also be used in research and development. The nitrophenyl group is a nitro-substituted aromatic ring that can be reactive and is often used in organic synthesis as an electrophile. The pyrrolidin-1-yl group is a five-membered heterocyclic ring that is commonly found in pharmaceutical compounds and has various biological activities. The methanone group is a functional group containing a carbonyl group bonded to a hydrogen atom. Due to its unique chemical properties and reactivity, (3-nitrophenyl)(pyrrolidin-1-yl)methanone has potential applications in the pharmaceutical and agricultural industries.

160647-67-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 160647-67-6 Structure
  • Basic information

    1. Product Name: (3-nitrophenyl)(pyrrolidin-1-yl)methanone
    2. Synonyms: (3-nitrophenyl)(pyrrolidin-1-yl)methanone;1-(3-nitrobenzoyl)pyrrolidine
    3. CAS NO:160647-67-6
    4. Molecular Formula: C11H12N2O3
    5. Molecular Weight: 220.22458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160647-67-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3-nitrophenyl)(pyrrolidin-1-yl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-nitrophenyl)(pyrrolidin-1-yl)methanone(160647-67-6)
    11. EPA Substance Registry System: (3-nitrophenyl)(pyrrolidin-1-yl)methanone(160647-67-6)
  • 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: 160647-67-6(Hazardous Substances Data)

160647-67-6 Usage

Uses

Used in Pharmaceutical Industry:
(3-nitrophenyl)(pyrrolidin-1-yl)methanone is used as an intermediate in the synthesis of pharmaceuticals for its reactivity and unique chemical properties. It can be used to develop new drugs with various biological activities.
Used in Agrochemical Industry:
(3-nitrophenyl)(pyrrolidin-1-yl)methanone is used as an intermediate in the synthesis of agrochemicals for its potential applications in developing new pesticides or other agricultural chemicals.
Used in Research and Development:
(3-nitrophenyl)(pyrrolidin-1-yl)methanone is used as a research compound to explore its unique chemical properties and reactivity, which can lead to the development of new applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 160647-67-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,6,4 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160647-67:
(8*1)+(7*6)+(6*0)+(5*6)+(4*4)+(3*7)+(2*6)+(1*7)=136
136 % 10 = 6
So 160647-67-6 is a valid CAS Registry Number.

160647-67-6Relevant articles and documents

METHODS OF CONTROLLING CROP PESTS USING AROMATIC AMIDE INSECT REPELLENTS, METHODS OF MAKING AROMATIC AMIDE INSECT REPELLENTS, AND NOVEL AROMATIC AMIDE INSECT REPELLENTS

-

Paragraph 0068-0069, (2022/03/18)

Methods of protecting fruit crops from flying insect pests and of repelling flying insects using aromatic amide compounds are disclosed. The methods apply the compounds to various surfaces, such as the fruit crops, the ground or structures adjacent to the fruit crops, or an object, article, human skin or animal. The compounds have the formula RxC6Hy—C(═O)—N(Cy), where RxC6Hy is a substituted phenyl group, each R group is independently C1-C6 alkyl, substituted C1-C4 alkyl, (substituted) C6-C10 aryl, C1-C4 alkoxy, C6-C10 aryloxy, halogen, nitro, cyano, cyanate, isocyanate, nitroso, C1-C4 alkylthio, phenylthio, (halogen-substituted) C1-C4 alkylsulfonyl, phenylsulfonyl, tolylsulfonyl, amino, mono- or di-C1-C4 alkylamino, diphenylamino, di-C1-C4 alkylamido, formyl, C2-C7 acyl, or C1-C6 alkoxycarbonyl; x is an integer of 1 to 5; x+y=5; Cy is a C2-C8 (substituted) alkadiyl, a C4-C6 (substituted) alkenediyl, or a (substituted) diyl of the formula —(CH2CH2)—O—(CH2CH2)—, —(CH2CH2)—NR′—(CH2CH2)— or —(CH2CH2)—S—(CH2CH2)— that, along with the amide N atom, forms a non-aromatic cyclic group; and R′ is C1-C6 alkyl, substituted C1-C4 alkyl, (substituted) C6-C10 aryl, or (substituted) benzyl.

Phenysilane and Silicon Tetraacetate: Versatile Promotors for Amide Synthesis

Morisset, Eléonore,Chardon, Aurélien,Rouden, Jacques,Blanchet, Jér?me

supporting information, p. 388 - 392 (2020/01/24)

Phenylsilane was reevaluated as a useful coupling reagent for amide synthesis. At room temperature, a wide range of amides and peptides were obtained in good to excellent yields (up to 99 %). For the first time, Weinreb amides synthesis mediated by a hydrosilane were also documented. Comparative experiments with various acetoxysilanes suggested the involvement of a phenyl-triacyloxysilane. From this mechanistic study, silicon tetraacetate was shown as an efficient amine acylating agent.

Direct allylation of aromatic and α,β-unsaturated carboxamides under ruthenium catalysis

Kim, Mirim,Sharma, Satyasheel,Mishra, Neeraj Kumar,Han, Sangil,Park, Jihye,Kim, Minyoung,Shin, Youngmi,Kwak, Jong Hwan,Han, Sang Hoon,Kim, In Su

supporting information, p. 11303 - 11306 (2014/11/07)

The ruthenium-catalyzed oxidative allylation of aromatic and α,β-unsaturated carboxamides with allylic carbonates is described. These transformations proceed readily with complete linear γ-selectivity of substituted allylic carbonates. the Partner Organisations 2014.

Novel Cyclic Urea Derivatives, Preparation Thereof and Pharmaceutical Use Thereof as Kinase Inhibitors

-

Page/Page column 48, (2009/04/24)

Compounds of formula (I): wherein Ra, Rb, R, X1 and X2 are as defined in the disclosure, pharmaceutical compositions comprising said compounds, processes for making and methods of using the same are provided.

IMIDAZO [1,2-A] PYRIDINES AND THEIR PHARMACEUTICAL USE

-

, (2008/06/13)

The invention relates to novel bradykinin antagonists of the formula: STR1 wherein R 1 is halogen,R 2 and R 3 are each hydrogen, lower alkyl, halo(lower)alkyl or acyl,R 4 is aryl having suitable substituent(s), or a heterocyclic group optionally having suitable substituent(s),Q is O or N--R 11, in which R 11 is hydrogen or acyl, andA is lower alkylene,and pharmaceutically acceptable salts thereof.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 160647-67-6