179894-36-1

• 

• Basic information

  1. Product Name: [1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid
  2. Synonyms:
  3. CAS NO:179894-36-1
  4. Molecular Formula: C₁₇H₂₄BNO₄
  5. Molecular Weight: 317.1878
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 179894-36-1.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 464.626°C at 760 mmHg
  3. Flash Point: 234.798°C
  4. Appearance: N/A
  5. Density: 1.17g/cm³
  6. Vapor Pressure: 0mmHg at 25°C
  7. Refractive Index: 1.56
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: [1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid(CAS DataBase Reference)
  11. NIST Chemistry Reference: [1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid(179894-36-1)
  12. EPA Substance Registry System: [1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid(179894-36-1)

• 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: 179894-36-1(Hazardous Substances Data)

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• Article

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• 179894-36-1

  Cas No: 179894-36-1

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• Suzhou Health Chemicals Co., Ltd.
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• 1(2H)-Quinolinecarboxylic acid, 6-borono-2,2,4-trimethyl-,1-(1,1-dimethylethyl) ester (9CI)

  Cas No: 179894-36-1

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• Henan Tianfu Chemical Co., Ltd.
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• (1-(tert-Butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl)boronic acid

  Cas No: 179894-36-1

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• ENAO Chemical Co, Limited
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• FT-0722602

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• Finetech Industry Limited
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• 1-(tert-butoxycarbonyl)-1,2-dihydro-2,2,4-trimethylquinolin-6-yl-6-boronic acid

  Cas No: 179894-36-1

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• Debye Scientific
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179894-36-1 Usage

General Description

[1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid is a chemical compound used in organic synthesis and medicinal chemistry. It is a boronic acid derivative with a quinoline core and a tert-butoxycarbonyl protecting group. The boronic acid functionality makes it useful as a building block in Suzuki-Miyaura cross-coupling reactions, which are important in the construction of carbon-carbon bonds. The quinoline core is a common structural motif found in many biologically active compounds, making this compound potentially useful in drug discovery and development. The tert-butoxycarbonyl protecting group provides stability and can be removed under mild conditions, making it a versatile tool in chemical synthesis. Overall, this compound has potential applications in both synthetic organic chemistry and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 179894-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,8,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 179894-36:
(8*1)+(7*7)+(6*9)+(5*8)+(4*9)+(3*4)+(2*3)+(1*6)=211
211 % 10 = 1
So 179894-36-1 is a valid CAS Registry Number.

179894-36-1SDS

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	[2,2,4-trimethyl-1-[(2-methylpropan-2-yl)oxycarbonyl]quinolin-6-yl]boronic acid

1.2 Other means of identification

Product number	-
Other names	I04-1404

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:179894-36-1 SDS

179894-36-1Upstream product

• 121-43-7 Trimethyl borate 
• 594-19-4 tert.-butyl lithium 
• 179894-35-0 6-Bromo-1-tert-butyloxycarbonyl-1,2-dihydro-2,2,4-trimethylquinoline 

179894-36-1Downstream Products

• 179896-16-3 6-(2-Amino-3,5-difluorophenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179896-07-2 6-(3-chloro-2-methylphenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179896-37-8 6-(5-Fluoro-2-methoxy-3-nitrophenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179897-79-1 1,2-Dihydro-2,2,4-trimethyl-6-[3-(methylsulfonyl)phenyl]quinoline 
• 179896-15-2 1,2-Dihydro-2,2,4-trimethyl-6-(2-methyl-3-nitrophenyl)quinoline 
• 179896-09-4 6-(3-Acetylphenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179896-19-6 6-(3-Fluoro-2-methylphenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179897-78-0 6-(3-Formylphenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179894-85-0 6-(3,5-Dichlorophenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179894-45-2 6-(2,3-Dichlorophenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179896-05-0 6-(3-Cyano-6-fluorophenyl)-1,2-dihydro-2,2,4-trimethylquinoline 
• 179894-87-2 1,2-Dihydro-2,2,4-trimethyl-6-(pentafluorophenyl)quinoline 
• 179896-06-1 6-[5-fluoro-3-(trifluoromethyl)phenyl]-1,2-dihydro-2,2,4-trimethylquinoline 
• 179894-86-1 6-(2,3-Difluorophenyl)-1,2-dihydro-2,2,4-trimethylquinoline 

179894-36-1Relevant articles and documents

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.

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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