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4-Fluorobenzyl-2,3,5,6-D4 Alcohol, with the chemical formula C7D4FH7O, is an isotopically labeled research compound. It is a deuterated and fluorinated derivative of benzyl alcohol, where four hydrogen atoms are replaced by deuterium (D) and one hydrogen atom on the benzene ring is replaced by fluorine (F). 4-FLUOROBENZYL-2,3,5,6-D4 ALCOHOL is commonly used in scientific research for various applications due to its unique properties.

93111-26-3

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93111-26-3 Usage

Uses

Used in Chemical Synthesis:
4-Fluorobenzyl-2,3,5,6-D4 Alcohol is used as an intermediate in the synthesis of various organic compounds. Its deuterated and fluorinated nature allows for the tracking and analysis of chemical reactions, providing valuable insights into reaction mechanisms and pathways.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Fluorobenzyl-2,3,5,6-D4 Alcohol serves as a valuable tool for drug discovery and development. Its isotopically labeled structure enables researchers to study the metabolism, pharmacokinetics, and pharmacodynamics of drug candidates, aiding in the optimization of drug design and efficacy.
Used in Analytical Chemistry:
4-Fluorobenzyl-2,3,5,6-D4 Alcohol is employed as a reference compound in analytical chemistry. Its unique isotopic signature allows for accurate quantification and identification of compounds in complex mixtures, making it useful in techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.
Used in Material Science:
In material science, 4-Fluorobenzyl-2,3,5,6-D4 Alcohol can be used to study the properties of various materials, such as polymers and coatings. Its incorporation into these materials can provide insights into their structure, stability, and performance, leading to the development of improved materials with enhanced properties.
Overall, 4-Fluorobenzyl-2,3,5,6-D4 Alcohol is a versatile isotopically labeled research compound with applications in various fields, including chemical synthesis, pharmaceutical research, analytical chemistry, and material science. Its unique properties make it a valuable tool for advancing scientific knowledge and developing new technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 93111-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93111-26:
(7*9)+(6*3)+(5*1)+(4*1)+(3*1)+(2*2)+(1*6)=103
103 % 10 = 3
So 93111-26-3 is a valid CAS Registry Number.

93111-26-3SDS

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 4-FLUOROBENZYL-2,3,5,6-D4 ALCOHOL

1.2 Other means of identification

Product number -
Other names 2,3,5,6-tetradeuterio-4-fluorobenzyl alcohol

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:93111-26-3 SDS

93111-26-3Relevant academic research and scientific papers

Dynamics at the Active Site of N2-Acetyl-N1-(4-fluorobenzyl)carbazoyl-α-chymotripsin

Gerig, J. T.,Hammond, S. J.

, p. 8244 - 8251 (2007/10/02)

N2-Acetyl-N1-(4-fluorobenzyl)carbazoyl-α-chymotrypsin is a catalytically inactive protein which should closely resemble the acylated enzyme intermediate formed during reaction of chymotripsin with substrates derived from phenylalanin

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