110969-45-4

• 

• Basic information

  1. Product Name: N-(TERT-BUTOXYCARBONYL)-2-ETHYLANILINE
  2. Synonyms: t-boc-2-ethylaniline;tert-butyl N-(2-ethylphenyl)carbamate
  3. CAS NO:110969-45-4
  4. Molecular Formula: C₁₃H₁₉NO₂
  5. Molecular Weight: 221.3
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 110969-45-4.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: 53-58 °C(lit.)
  2. Boiling Point: 80-90 °C0.5 mm Hg(lit.)
  3. Flash Point: 117.8°C
  4. Appearance: /
  5. Density: 1.047g/cm³
  6. Vapor Pressure: 0.00653mmHg at 25°C
  7. Refractive Index: 1.534
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 13.87±0.70(Predicted)
  11. CAS DataBase Reference: N-(TERT-BUTOXYCARBONYL)-2-ETHYLANILINE(CAS DataBase Reference)
  12. NIST Chemistry Reference: N-(TERT-BUTOXYCARBONYL)-2-ETHYLANILINE(110969-45-4)
  13. EPA Substance Registry System: N-(TERT-BUTOXYCARBONYL)-2-ETHYLANILINE(110969-45-4)

• Safety Data

  1. Hazard Codes: Xi
  2. Statements: 36/37/38
  3. Safety Statements: 26-36
  4. WGK Germany: 3
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 110969-45-4(Hazardous Substances Data)

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• N-(tert-Butoxycarbonyl)-2-ethylaniline

  Cas No: 110969-45-4

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• Dayang Chem (Hangzhou) Co.,Ltd.
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• TIANFUCHEM-Carbamic acid,N-(2-ethylphenyl)-, 1,1-dimethylethyl ester

  Cas No: 110969-45-4

• USD $ 2000.0-2000.0 / Metric Ton

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110969-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110969-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,6 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110969-45:
(8*1)+(7*1)+(6*0)+(5*9)+(4*6)+(3*9)+(2*4)+(1*5)=124
124 % 10 = 4
So 110969-45-4 is a valid CAS Registry Number.

InChI:InChI=1/C13H19NO2/c1-5-10-8-6-7-9-11(10)14-12(15)16-13(2,3)4/h6-9H,5H2,1-4H3,(H,14,15)

110969-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	tert-butyl N-(2-ethylphenyl)carbamate

1.2 Other means of identification

Product number	-
Other names	N-Boc-2-ethylaniline

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:110969-45-4 SDS

110969-45-4Upstream product

• 109774-64-3 Acetyl-(4-tert-butyl-phenyl)-carbamic acid tert-butyl ester 
• 578-54-1 ortho-ethylaniline 
• 24424-99-5 di-tert-butyl dicarbonate 

110969-45-4Downstream Products

• 314773-77-8 tert-butyl (2-acetylphenyl)carbamate 
• 1035225-97-8 C₂₀H₃₁NO₃ 
• 1504-06-9 3-methylindolin-2-one 
• 1301630-30-7 1,1-dimethylethyl N-(2-ethylphenyl)-N-methyl-carbamate 
• 1301630-31-8 1,1-dimethylethyl N-(2-ethylphenyl)-N-[(methylthio)methyl]carbamate 
• 1301630-32-9 C₁₅H₂₃NO₂S 

110969-45-4Relevant articles and documents

Preparation of indoles and oxindoles from N-(tert-butoxycarbonyl)-2-alkylanilines

Clark,Muchowski,Fisher,Flippin,Repke,Souchet

, p. 871 - 878 (2007/10/02)

Treatment of dilithiated N-(tert-butoxycarbonyl)anilines 1 with dimethylformamide or carbon dioxide furnishes intermediates 3, 5, that are easily converted to N-(tert-butoxycarbonyl)indoles 4 and oxindoles (indol-2(3H)-ones, 7), respectively. Condensation of dilithiated 1 with N-methoxy-N-methylamides provides ketones 9 which are cyclized upon trifluoroacetic acid treatment to either 2-substituted 1-(tert-butoxycarbonyl)indoles 10 or 2-substituted indoles 11 depending on the reaction time. This general methodology has been applied to efficient synthesis of 1,2-alkyl-bridged indoles 12, 1,3,4,5-tetrahydrobenz[c,d]indole (16), 2a,3,4,5-tetrahydrobenz[c,d]indol-2(1H)-one (18), and 1-(tert-butoxycarbonyl)1H-pyrrolo[2,3-b]pyridine (21).

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