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Benzenemethanol, 4-methoxy-a-(1-methylpropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14248-29-4

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14248-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14248-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,4 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14248-29:
(7*1)+(6*4)+(5*2)+(4*4)+(3*8)+(2*2)+(1*9)=94
94 % 10 = 4
So 14248-29-4 is a valid CAS Registry Number.

14248-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-2-methyl-1-(4-methoxy-phenyl)-butane

1.2 Other means of identification

Product number -
Other names Opt.-inakt. 4-Methoxy-1-(1-hydroxy-2-methyl-butyl)-benzol

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:14248-29-4 SDS

14248-29-4Relevant academic research and scientific papers

Electrochemical alkyl transfer reactions of trialkylborane to carbonyl compounds by use of copper sacrificial anode

Choi, Jung Hoon,Youm, Jong Sung,Cho, Cheon-Gyu,Czae, Myung-Zoon,Hwang, Book Kee,Kim, Jung Sung

, p. 4835 - 4838 (2007/10/03)

Alkyl groups in trialkylboranes were successfully transferred to carbonyl compounds in the presence of the platinum cathode and copper anode by electrochemical method. The new, mild electrochemical alkyl transfer reaction produced various substituted alcohols in good yields.

Influence of Alkyl Chain Ramification on Estradiol Receptor Binding Affinity and Intrinsic Activity of 1,2-Dialkylated 1,2-Bis(4- or 3-hydroxyphenyl)ethane Estrogens and Antiestrogens

Hartmann, Rolf W.

, p. 1668 - 1674 (2007/10/02)

The influence of a symmetrical introduction of CH3 substituents in the α or β positions of the 1,2-dialkyl-1,2-bis(4-hydroxyphenyl)ethene estrogens hexestrol (ethyl, HES) and octestrol (n-propyl, OCES) isopropyl (1), tert-butyl (2), sec-butyl (3), isobut

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