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1H-Benzimidazole-2-methanamine,5-nitro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115103-10-1 Structure
  • Basic information

    1. Product Name: 1H-Benzimidazole-2-methanamine,5-nitro-(9CI)
    2. Synonyms: 1H-Benzimidazole-2-methanamine,5-nitro-(9CI)
    3. CAS NO:115103-10-1
    4. Molecular Formula: C8H8N4O2
    5. Molecular Weight: 192.17472
    6. EINECS: N/A
    7. Product Categories: BENZIMIDAZOLE
    8. Mol File: 115103-10-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 486.7±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.514±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 11.81±0.29(Predicted)
    10. CAS DataBase Reference: 1H-Benzimidazole-2-methanamine,5-nitro-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Benzimidazole-2-methanamine,5-nitro-(9CI)(115103-10-1)
    12. EPA Substance Registry System: 1H-Benzimidazole-2-methanamine,5-nitro-(9CI)(115103-10-1)
  • 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: 115103-10-1(Hazardous Substances Data)

115103-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115103-10-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,0 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115103-10:
(8*1)+(7*1)+(6*5)+(5*1)+(4*0)+(3*3)+(2*1)+(1*0)=61
61 % 10 = 1
So 115103-10-1 is a valid CAS Registry Number.

115103-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-nitro-1H-benzo[d]imidazol-2-yl)methanamine

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:115103-10-1 SDS

115103-10-1Downstream Products

115103-10-1Relevant articles and documents

Synthesis and biological activity of squaramido-tethered bisbenzimidazoles as synthetic anion transporters

Wang, Zhong-Kun,Hong, Xiao-Qiao,Hu, Jinhui,Xing, Yuan-Yuan,Chen, Wen-Hua

, p. 3972 - 3980 (2021)

A series of squaramido-tethered bisbenzimidazoles were synthesized from the reaction of diethyl squarate with substituted 2-aminomethylbenzimidazoles. These conjugates exhibit moderate binding affinity toward chloride anions. They are able to facilitate the transmembrane transport of chloride anions most probably via an anion exchange process, and tend to be more active at acidic pH than at physiological pH. The viability of these conjugates toward four selected solid tumor cell lines was evaluated using an MTT assay and the results suggest that some of these conjugates exhibit moderate cytotoxicity probably in an apoptotic fashion.

Dibenzimidazole conjugates with pH dependent anion trans-membrane transport activity Synthesis method and synthesis method thereof (by machine translation)

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Paragraph 0072-0080; 0084, (2021/01/04)

13-bis-benzimidazole conjugate is synthesized by the method, the chloride ion transport activity of each conjugate under the acidic pH condition is higher than the activity at physiological pH, and the synthesized conjugate also shows moderate intensity toxicity on selected solid tumor cells. (by machine translation)

POTENT SMALL MOLECULE INHIBITORS OF AUTOPHAGY, AND METHODS OF USE THEREOF

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Page/Page column 123, (2014/09/29)

Certain aspects of the invention relate to small molecule autophagy inhibitors, and their use for treatment and prevention of cancers and acute pancreatitis. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity.

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