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tert-butyl 2-(5-broMopyridin-3-yl)pyrrolidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 179120-81-1 Structure
  • Basic information

    1. Product Name: tert-butyl 2-(5-broMopyridin-3-yl)pyrrolidine-1-carboxylate
    2. Synonyms: tert-butyl 2-(5-broMopyridin-3-yl)pyrrolidine-1-carboxylate
    3. CAS NO:179120-81-1
    4. Molecular Formula: C14H19BrN2O2
    5. Molecular Weight: 327.21686
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 179120-81-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 388.2±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.360±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.81±0.22(Predicted)
    10. CAS DataBase Reference: tert-butyl 2-(5-broMopyridin-3-yl)pyrrolidine-1-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: tert-butyl 2-(5-broMopyridin-3-yl)pyrrolidine-1-carboxylate(179120-81-1)
    12. EPA Substance Registry System: tert-butyl 2-(5-broMopyridin-3-yl)pyrrolidine-1-carboxylate(179120-81-1)
  • 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: 179120-81-1(Hazardous Substances Data)

179120-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 179120-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,1,2 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 179120-81:
(8*1)+(7*7)+(6*9)+(5*1)+(4*2)+(3*0)+(2*8)+(1*1)=141
141 % 10 = 1
So 179120-81-1 is a valid CAS Registry Number.

179120-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 2-(5-bromopyridin-3-yl)pyrrolidine-1-carboxylate

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:179120-81-1 SDS

179120-81-1Relevant articles and documents

Benzophenones as inhibitors of IL-1beta and TNF-alpha

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, (2008/06/13)

Heteroaryl aminobenzophenones of general formula I inhibit interleukin-1β and TNF-α and may therefore be useful in the therapy of inflammatory diseases and conditions.

MODULATORS OF ACETYLCHOLINE RECEPTORS

-

, (2008/06/13)

The present invention provides a class of pyridine compounds which are modulators of acetylcholine receptors, i.e., compounds which displace acetylcholine receptor ligands from their binding sites. Invention compounds may act as agonists, partial agonists

MODULATORS OF ACETYLCHOLINE RECEPTORS

-

, (2008/06/13)

The present invention provides a class of pyridine compounds which are modulators of acetylcholine receptors, i.e., compounds which displace acetylcholine receptor ligands from their binding sites. Invention compounds may act as agonists, partial agonists

METHODS FOR THE PREPARATION OF MODULATORS OF ACETYLCHOLINE RECEPTORS

-

, (2008/06/13)

In accordance with the present invention, there is provided a class of pyridine compounds which are modulators of acetylcholine receptors. The compounds of the invention displace acetylcholine receptor ligands from their binding sites. Invention compounds

Modulators of acetylcholine receptors

-

, (2008/06/13)

In accordance with the present invention, there is provided a class of pyridine compounds which are modulators of acetylcholine receptors. The compounds of the invention displace acetylcholine receptor ligands from their binding sites. Invention compounds

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