138948-58-0

• 

• Basic information

  1. Product Name: Benzenemethanol, -alpha--methyl-4-(2-methylpropyl)-, acetate (9CI)
  2. Synonyms: Benzenemethanol, -alpha--methyl-4-(2-methylpropyl)-, acetate (9CI)
  3. CAS NO:138948-58-0
  4. Molecular Formula: C₁₄H₂₀O₂
  5. Molecular Weight: 220.3074
  6. EINECS: N/A
  7. Product Categories: ACIDHALIDE
  8. Mol File: 138948-58-0.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Benzenemethanol, -alpha--methyl-4-(2-methylpropyl)-, acetate (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Benzenemethanol, -alpha--methyl-4-(2-methylpropyl)-, acetate (9CI)(138948-58-0)
  11. EPA Substance Registry System: Benzenemethanol, -alpha--methyl-4-(2-methylpropyl)-, acetate (9CI)(138948-58-0)

• 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: 138948-58-0(Hazardous Substances Data)

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138948-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138948-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,4 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138948-58:
(8*1)+(7*3)+(6*8)+(5*9)+(4*4)+(3*8)+(2*5)+(1*8)=180
180 % 10 = 0
So 138948-58-0 is a valid CAS Registry Number.

138948-58-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	(RS)-p-isobutyl-1-phenylethanol acetate

1.2 Other means of identification

Product number	-
Other names	Acetic acid 1-(4-isobutyl-phenyl)-ethyl ester

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:138948-58-0 SDS

138948-58-0Upstream product

• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 15687-27-1 ibuprofen 
• 142-71-2 copper diacetate 
• 64-19-7 acetic acid 
• 40150-92-3 1-(4-isobutylphenyl)ethanol 
• 108-24-7 acetic anhydride 
• 108-05-4 vinyl acetate 

138948-58-0Downstream Products

• 125653-66-9 (S)-(-)-1-(4-isobutylphenyl)ethanol 
• 130007-66-8 R-(-)-2-(4-isobutyl-phenyl)-2-hydroxyethane 
• 125653-69-2 Acetic acid (S)-1-(4-isobutyl-phenyl)-ethyl ester 
• 40150-92-3 1-(4-isobutylphenyl)ethanol 
• 148366-88-5 ethyl (S)-4-[3-[4-[[1-(4-isobutylphenyl)ethyl]oxy]benzoyl]-1H-indol-1-yl]butyrate 

138948-58-0Relevant articles and documents

Decarboxylative Acetoxylation of Aliphatic Carboxylic Acids

Senaweera, Sameera,Cartwright, Kaitie C.,Tunge, Jon A.

, p. 12553 - 12561 (2019/10/14)

Organic molecules bearing acetoxy moieties are important functionalities in natural products, drugs, and agricultural chemicals. Synthesis of such molecules via transition metal-catalyzed C-O bond formation can be achieved in the presence of a carefully chosen directing group to alleviate the challenges associated with regioselectivity. An alternative approach is to use ubiquitous carboxylic acids as starting materials and perform a decarboxylative coupling. Herein, we report conditions for a photocatalytic decarboxylative C-O bond formation reaction that provides rapid and facile access to the corresponding acetoxylated products. Mechanistic investigations suggest that the reaction operates via oxidation of the carboxylate followed by rapid decarboxylation and oxidation by Cu(OAc)2

Highly enantioselective aminoacylase-catalyzed transesterification of secondary alcohols

Bakker,Spruijt,Van Rantwijk,Sheldon

, p. 1801 - 1808 (2007/10/03)

The aminoacylase (N-acyl-L-amino acid amidohydrolase; E.C. 3.5.1.14) from Aspergillus melleus, a readily available inexpensive enzyme, catalyzes the transesterification of a wide range of chiral secondary arylalkanols with essentially absolute stereoselectivity (E> 500). Moreover, the productivities obtained with 1-phenylethanol, 1-phenylpropanol, 1-(1-naphthyl)ethanol and 1- (2-naphthyl)ethanol were substantially higher than those in the corresponding lipase-catalyzed transesterifications. (C) 2000 Elsevier Science Ltd.

LIPASE-CATALYZED IRREVERSIBLE TRANSESTERIFICATION USING ENOL ESTERS: XAD-8 IMMOBILIZED LIPOPROTEIN LIPASE-CATALYZED RESOLUTION OF SECONDARY ALCOHOLS

Hsu, Shu-Hui,Wu, Shihn-Sheng,Wang, Yi-Fong,Wong, Chi-Huey

, p. 6403 - 6406 (2007/10/02)

Procedures for preparation of XAD-8 immobilized lipoprotein lipase and the resolution of secondary alcohols of synthetic value in organic solvents using this immobilized enzyme have been developed.

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