19271-90-0

• 

• Basic information

  1. Product Name: (2-TERT-BUTYLPHENOXY)ACETIC ACID
  2. Synonyms: Aceticacid, (o-tert-butylphenoxy)- (6CI,8CI);Acetic acid,[2-(1,1-dimethylethyl)phenoxy]- (9CI);(2-tert-Butylphenoxy)acetic acid;[2-(1,1-Dimethylethyl)phenoxy]ethanoic acid;ZINC04206272;AC1OFIKH;CID7129047;2-(2-Tert-butylphenoxy)acetate;
  3. CAS NO:19271-90-0
  4. Molecular Formula: C₁₂H₁₆O₃
  5. Molecular Weight: 208.26
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 19271-90-0.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: 140.0-141.0 °C
  2. Boiling Point: 330.9 °C at 760 mmHg
  3. Flash Point: 123.5 °C
  4. Appearance: /
  5. Density: 1.088±0.06 g/cm3(Predicted)
  6. Vapor Pressure: 6.44E-05mmHg at 25°C
  7. Refractive Index: N/A
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 3.23±0.10(Predicted)
  11. CAS DataBase Reference: (2-TERT-BUTYLPHENOXY)ACETIC ACID(CAS DataBase Reference)
  12. NIST Chemistry Reference: (2-TERT-BUTYLPHENOXY)ACETIC ACID(19271-90-0)
  13. EPA Substance Registry System: (2-TERT-BUTYLPHENOXY)ACETIC ACID(19271-90-0)

• 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: 19271-90-0(Hazardous Substances Data)

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• Acetic acid,2-[2-(1,1-dimethylethyl)phenoxy]-

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• Acetic acid,2-[2-(1,1-dimethylethyl)phenoxy]-

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19271-90-0 Usage

Uses

(2-tert-butylphenoxy)acetic acid is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 19271-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19271-90:
(7*1)+(6*9)+(5*2)+(4*7)+(3*1)+(2*9)+(1*0)=120
120 % 10 = 0
So 19271-90-0 is a valid CAS Registry Number.

InChI:InChI=1/C12H16O3/c1-12(2,3)9-6-4-5-7-10(9)15-8-11(13)14/h4-7H,8H2,1-3H3,(H,13,14)/p-1

19271-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-(2-tert-butylphenoxy)acetic acid

1.2 Other means of identification

Product number	-
Other names	O-T-butylphenoxyacetic acid

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:19271-90-0 SDS

19271-90-0Upstream product

• 88-18-6 2-tert-Butylphenol 
• 79-11-8 chloroacetic acid 
• 787575-52-4 (2-tert-butyl-phenoxy)-acetic acid methyl ester 
• 1433755-40-8 C₁₆H₂₄O₃ 

19271-90-0Downstream Products

• 278597-91-4 tert-butyl (2S)-2-{[(2S)-2-({2-[2-(tert-butyl)phenoxy]acetyl}amino)-4-methylpentanoyl]amino}-3-(4-hydroxyphenyl)propanoate 
• 1435933-35-9 C₂₀H₂₇N₃O₃ 
• 953755-12-9 N-(4-aminophenyl)-2-(2-(tert-butyl)phenoxy)acetamide 

19271-90-0Relevant articles and documents

Discovery of potent transient receptor potential vanilloid 1 antagonists: Design and synthesis of phenoxyacetamide derivatives

Takahashi, Eiki,Hirano, Noriyuki,Nagahara, Takashi,Yoshikawa, Satoru,Momen, Shinobu,Yokokawa, Hiroshi,Hayashi, Ryoji

, p. 3154 - 3156 (2013/06/26)

We aimed to discover a novel type of transient receptor potential vanilloid 1 (TRPV1) antagonist because such antagonists are possible drug candidates for treating various disorders. We modified the structure of hit compound 7 (human TRPV1 IC50 = 411 nM) and converted its pyrrolidino group to a (hydroxyethyl)methylamino group, which substantially improved inhibitory activity (15d; human TRPV1 IC50 = 33 nM). In addition, 15d ameliorated bladder overactivity in rats in vivo.

Solvent-free synthesis of substituted phenoxyacetic acids under microwave irradiation

Nagy, Gabriela,Filip, Sorin V.,Surducan, Emanoil,Surducan, Vasile

, p. 3729 - 3736 (2007/10/03)

A comparison of microwave-activated vs. classical organic synthesis is presented for a variety of growth-regulator compounds with a phenoxyacetic acid structure. Microwave-assisted nucleophilic substitutions are safely and conveniently carried out in an open vessel, without any solvent. Yields are very good, and reaction times are extremely short.

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