179894-35-0

• 

• Basic information

  1. Product Name: tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate
  2. Synonyms: tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate
  3. CAS NO:179894-35-0
  4. Molecular Formula: C₁₇H₂₂BrNO₂
  5. Molecular Weight: 352.27
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 179894-35-0.mol
  9. Article Data: 9

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 402.175°C at 760 mmHg
  3. Flash Point: 197.028°C
  4. Appearance: /
  5. Density: 1.256g/cm³
  6. Vapor Pressure: 0mmHg at 25°C
  7. Refractive Index: 1.541
  8. Storage Temp.: 2-8°C
  9. Solubility: N/A
  10. CAS DataBase Reference: tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate(CAS DataBase Reference)
  11. NIST Chemistry Reference: tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate(179894-35-0)
  12. EPA Substance Registry System: tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate(179894-35-0)

• 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: 179894-35-0(Hazardous Substances Data)

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• SDS
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• Article

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• Suzhou Health Chemicals Co., Ltd.
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• tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate

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• tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate

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• tert-Butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate

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179894-35-0 Usage

General Description

Tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate is a chemical compound with the molecular formula C16H22BrNO2. It is a quinoline derivative with a tert-butyl ester group attached to the carboxylate functionality, as well as a bromine atom at the 6th position of the quinoline ring. tert-butyl 6-bromo-2,2,4-trimethylquinoline-1(2H)-carboxylate is commonly used in organic synthesis and as a building block for the preparation of various pharmaceuticals and agrochemicals due to its unique structural features and reactivity. Additionally, its tert-butyl ester group provides increased stability and protection against hydrolysis in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 179894-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,8,9 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 179894-35:
(8*1)+(7*7)+(6*9)+(5*8)+(4*9)+(3*4)+(2*3)+(1*5)=210
210 % 10 = 0
So 179894-35-0 is a valid CAS Registry Number.

InChI:InChI=1/C17H22BrNO2/c1-11-10-17(5,6)19(15(20)21-16(2,3)4)14-8-7-12(18)9-13(11)14/h7-10H,1-6H3

179894-35-0SDS

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 6-bromo-2,2,4-trimethylquinoline-1-carboxylate

1.2 Other means of identification

Product number	-
Other names	I08-0442

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:179894-35-0 SDS

179894-35-0Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 91720-32-0 6-bromo-2,2,4-trimethyl-1,2-dihydroquinoline 
• 109-72-8 n-butyllithium 
• 106-40-1 4-bromo-aniline 

179894-35-0Downstream Products

• 179894-42-9 6-(4-Fluorophenyl)-1,2,dihydro-2,2,4-trimethylquinoline 
• 179894-43-0 1,2-Dihydro-6-(3-trifluoromethylphenyl)-2,2,4-trimethylquinoline 
• 179898-09-0 methyl (5'-fluoro-2'-methoxy-4-nitro-2-biphenyl)carboxylate 
• 179894-36-1 (1-tert-butyloxycarbonyl-1,2-dihydro-2,2,4-trimethyl-6-quinolinyl)boronic acid 

179894-35-0Relevant articles and documents

AROMATIC SULFONE COMPOUND AS ALDOSTERONE RECEPTOR MODULATOR

-

Page/Page column 34, (2010/11/28)

The present invention provides a compound represented by the following formula (I): [wherein, A represents a group of the following formula (A-1): etc., R1 and R2 each independently represent a hydrogen atom etc., Z represents CR3 etc., W represents CR4 etc., Q represents CR5 etc., R3, R4 and R5 each independently represent a hydrogen atom etc., Y represents an oxygen atom or sulfur atom, X represents an oxygen atom etc. and B represents an optionally substituted aryl group or optionally substituted heteroaryl group], the prodrug thereof or the pharmaceutically acceptable salt thereof for preventing or treating various diseases such as hypertesion, cerebral stroke, cardiac failure, etc.

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

Steroid receptor modulator compounds and methods

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

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