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3-(4-TERT-BUTYL-PHENYL)-PROPAN-1-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78574-08-0 Structure
  • Basic information

    1. Product Name: 3-(4-TERT-BUTYL-PHENYL)-PROPAN-1-OL
    2. Synonyms: 3-(4-TERT-BUTYL-PHENYL)-PROPAN-1-OL
    3. CAS NO:78574-08-0
    4. Molecular Formula: C13H20O
    5. Molecular Weight: 192.2973
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78574-08-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 291°C at 760 mmHg
    3. Flash Point: 114.5°C
    4. Appearance: /
    5. Density: 0.947g/cm3
    6. Vapor Pressure: 0.000919mmHg at 25°C
    7. Refractive Index: 1.506
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(4-TERT-BUTYL-PHENYL)-PROPAN-1-OL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(4-TERT-BUTYL-PHENYL)-PROPAN-1-OL(78574-08-0)
    12. EPA Substance Registry System: 3-(4-TERT-BUTYL-PHENYL)-PROPAN-1-OL(78574-08-0)
  • 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: 78574-08-0(Hazardous Substances Data)

78574-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78574-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78574-08:
(7*7)+(6*8)+(5*5)+(4*7)+(3*4)+(2*0)+(1*8)=170
170 % 10 = 0
So 78574-08-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O/c1-13(2,3)12-8-6-11(7-9-12)5-4-10-14/h6-9,14H,4-5,10H2,1-3H3

78574-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-tert-butylphenyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names Benzenepropanol,4-(1,1-dimethylethyl)

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:78574-08-0 SDS

78574-08-0Relevant articles and documents

Access to Trisubstituted Fluoroalkenes by Ruthenium-Catalyzed Cross-Metathesis

Nouaille, Augustin,Pannecoucke, Xavier,Poisson, Thomas,Couve-Bonnaire, Samuel

supporting information, p. 2140 - 2147 (2021/03/06)

Although the olefin metathesis reaction is a well-known and powerful strategy to get alkenes, this reaction remained highly challenging with fluororalkenes, especially the Cross-Metathesis (CM) process. Our thought was to find an easy accessible, convenient, reactive and post-functionalizable source of fluoroalkene, that we found as the methyl 2-fluoroacrylate. We reported herein the efficient ruthenium-catalyzed CM reaction of various terminal and internal alkenes with methyl 2-fluoroacrylate giving access, for the first time, to trisubstituted fluoroalkenes stereoselectively. Unprecedent TON for CM involving fluoroalkene, up to 175, have been obtained and the reaction proved to be tolerant and effective with a large range of olefin partners giving fair to high yields in metathesis products. (Figure presented.).

Iridium Complex-Catalyzed C2-Extension of Primary Alcohols with Ethanol via a Hydrogen Autotransfer Reaction

Kobayashi, Masaki,Itoh, Satoshi,Yoshimura, Keisuke,Tsukamoto, Yuya,Obora, Yasushi

, p. 11952 - 11958 (2020/10/23)

The development of a C2-extension of primary alcohols with ethanol as the C2 source and catalysis by [Cp*IrCl2]2 (where Cp? = pentamethylcyclopentadiene) is described. This new extension system was used for a range of benzylic alcohol substrates and for aliphatic alcohols with ethanol as an alkyl reagent to generate the corresponding C2-extended linear alcohols. Mechanistic studies of the reaction by means of intermediates and deuterium labeling experiments suggest the reaction is based on hydrogen autotransfer.

Palladium-catalyzed double-bond migration of unsaturated hydrocarbons accelerated by tantalum chloride

Murai, Masahito,Nishimura, Kengo,Takai, Kazuhiko

supporting information, p. 2769 - 2772 (2019/03/23)

The operationally simple palladium-catalyzed double-bond migration without heteroatom-containing coordinating functional groups is described. Addition of TaCl5 as a second catalyst greatly enhanced the migration efficiency to provide β-alkylsty

4“-O-Alkylated α-Galactosylceramide Analogues as iNKT-Cell Antigens: Synthetic, Biological, and Structural Studies

Janssens, Jonas,Bitra, Aruna,Wang, Jing,Decruy, Tine,Venken, Koen,van der Eycken, Johan,Elewaut, Dirk,Zajonc, Dirk M.,van Calenbergh, Serge

, p. 147 - 168 (2019/01/04)

Invariant natural killer T-cells (iNKT) are a glycolipid-responsive subset of T-lymphocytes that fulfill a pivotal role in the immune system. The archetypical synthetic glycolipid, α-galactosylceramide (α-GalCer), whose molecular framework is inspired by

Anodic benzylic C(sp3)-H amination: Unified access to pyrrolidines and piperidines

Herold, Sebastian,Bafaluy, Daniel,Mu?iz, Kilian

, p. 3191 - 3196 (2018/07/29)

An electrochemical aliphatic C-H amination strategy was developed to access the important heterocyclic motifs of pyrrolidines and piperidines within a uniform reaction protocol. The mechanism of this unprecedented C-H amination strategy involves anodic C-H activation to generate a benzylic cation, which is efficiently trapped by a nitrogen nucleophile. The applicability of the process is demonstrated for 40 examples comprising both 5- and 6-membered ring formations.

Aromatic compounds and their use in perfumery

-

, (2008/06/13)

The compounds of formula STR1 wherein symbol X represents a --CHO group or an acetal group of formula STR2 symbols R', taken separately, represent each a C1 to C4, linear or branched, saturated or unsaturated, hydrocarbon radical or, taken together, represent a C1 to C4 alkylene radical, which may be substituted, and symbol R represents a hydrogen atom or a methyl radical, are useful as perfuming ingredients for the preparation of perfuming compositions and perfumed articles, to which they impart floral type notes.

DECARBOXYLATIVE PHOTOOXYGENATION OF CARBOXYLIC ACIDS BY THE USE OF ACRIDINE

Okada, Keiji,Okubo, Katsura,Oda, Masaji

, p. 83 - 84 (2007/10/02)

A new method of decarboxylative photooxygenation of free carboxylic acids is developed by the use of acridine as a light absorber, leading to alcohols after reductive treatment of the photolysate.

N-disubstituted cycloalkylmethyl amines useful as fungicides

-

, (2008/06/13)

Compounds having plant fungicidal properties are of formula: and stereoisomers thereof, wherein R1 and R2, each represent a hydrogen atom, a halogen atom, or an alkyl group containing from 1 to 4 carbon atoms, R3 and Rsub

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