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ETHYL 3-NITRO-4-(PROPYLAMINO)BENZOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 312922-00-2 Structure
  • Basic information

    1. Product Name: ETHYL 3-NITRO-4-(PROPYLAMINO)BENZOATE
    2. Synonyms: ETHYL 3-NITRO-4-(PROPYLAMINO)BENZOATE
    3. CAS NO:312922-00-2
    4. Molecular Formula: C12H16N2O4
    5. Molecular Weight: 252.26644
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 312922-00-2.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: ETHYL 3-NITRO-4-(PROPYLAMINO)BENZOATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: ETHYL 3-NITRO-4-(PROPYLAMINO)BENZOATE(312922-00-2)
    11. EPA Substance Registry System: ETHYL 3-NITRO-4-(PROPYLAMINO)BENZOATE(312922-00-2)
  • 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: 312922-00-2(Hazardous Substances Data)

312922-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312922-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,9,2 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 312922-00:
(8*3)+(7*1)+(6*2)+(5*9)+(4*2)+(3*2)+(2*0)+(1*0)=102
102 % 10 = 2
So 312922-00-2 is a valid CAS Registry Number.

312922-00-2SDS

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 ethyl 3-nitro-4-(propylamino)benzoate

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:312922-00-2 SDS

312922-00-2Relevant articles and documents

In vitro, in vivo and in silico-driven identification of novel benzimidazole derivatives as anticancer and anti-inflammatory agents

Chandrashekarappa, Revanasiddappa B.,Merugumolu, Vijay K.,Poojary, Boja,Rangappa, Shobith,Sathyanarayana, Reshma,Srinivasa, Sudhanva M.

, (2021/08/24)

The synthesis of novel benzimidazole derivatives with varied carbon chain length was achieved via “one-pot” nitro reductive cyclization (6a–o). In each case, compounds were determined by the elemental analyses, FT-IR, mass, 1H and 13

Novel [1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives embedded with benzimidazole moiety as potent antioxidants

Sathyanarayana, Reshma,Poojary, Boja,Chandrashekarappa, Revanasiddappa B.,Kumar, Hemanth,Merugumolu, Vijay K.

, p. 1501 - 1516 (2020/04/15)

Fourteen novel [1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives bearing benzimidazole moiety (7a-n) have been synthesized using the one-pot nitro reductive cyclization method. All the synthesized compounds were confirmed by 1H nuclear magne

Microwave-assisted synthesis of benzimidazole derivatives through nitro reductive cyclization and their biological study

Manju,Kalluraya, Balakrishna,Asma,Kumar, Madan S

, p. 415 - 422 (2018/09/25)

A simple, effective, and eco-friendly synthesis of new benzimidazole-bearing aromatic/heteroaromatic compounds (4 a-o) using sodium dithionite as an effective reductive cyclizing reagent in dimethyl sulfoxide under microwave method is described. The newly

Synthesis and potent antimicrobial activity of some novel methyl or ethyl 1H-benzimidazole-5-carboxylates derivatives carrying amide or amidine groups

Oezden, Seckin,Atabey, Dilek,Yildiz, Sulhiye,Goeker, Hakan

, p. 1587 - 1597 (2007/10/03)

A series of benzimidazole-5-carboxylic acid alkyl ester derivatives carrying amide or amidine substituted methyl or phenyl groups at the position C-2 were synthesised and evaluated for antibacterial and antifungal activities against S. aureus, methicillin

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