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38923-38-5

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38923-38-5 Usage

General Description

3-(Trifluoromethyl)phenylglyoxal hydrate is a chemical compound, which is often used as a reagent in the synthesis of various other chemicals. Notably, it is used in the preparation of amides and trifluoromethyl-phenylhydrazones that have potential biological applications. Its exact structure consists of a phenyl ring, which is a six-carbon ring bonded with alternating single and double bonds, attached to a glyoxal group, and a trifluoromethyl group. The presence of the three fluorine atoms makes this compound significantly more reactive. No specific data is immediately available about its health effects or safety handling procedures, suggesting that it should be handled with general chemical safety standards in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 38923-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38923-38:
(7*3)+(6*8)+(5*9)+(4*2)+(3*3)+(2*3)+(1*8)=145
145 % 10 = 5
So 38923-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H5F3O2.H2O/c10-9(11,12)7-3-1-2-6(4-7)8(14)5-13;/h1-5H;1H2

38923-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-2-[3-(trifluoromethyl)phenyl]acetaldehyde,hydrate

1.2 Other means of identification

Product number -
Other names (3-trifluoromethylphenyl)(oxo)acetaldehyde

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:38923-38-5 SDS

38923-38-5Relevant articles and documents

Thiadiazole amide compound and application thereof

-

Paragraph 0088; 0865-0870, (2021/09/29)

The invention discloses a thiadiazole amide compound and application thereof, and belongs to the field of medicines. The structural general formula of the compound is shown as a formula (I) and is a novel compound with androgen receptor antagonistic activity, wherein one of the key targets is a binding pocket between the androgen receptor ligand binding domain dimer interface. The compound provided by the invention has high activity for antagonizing the transcription of androgen receptor and is at the molecular level. The cell level and the animal level all show good biological activity, and have better safety. , The invention can be applied to the preparation of drugs for treating androgen receptor abnormal expression tumors, including but not limited to prostate cancer, metastatic prostate cancer, castration-resistant prostate cancer, breast cancer and ovarian cancer.

Unexplored reactivity of 2-oxoaldehydes towards Pictet-Spengler conditions: Concise approach to β-carboline based marine natural products

Battini, Narsaiah,Padala, Anil K.,Mupparapu, Nagaraju,Vishwakarma, Ram A.,Ahmed, Qazi Naveed

, p. 26258 - 26263 (2014/07/08)

Novel reactions under Pictet-Spengler conditions between tryptophan methyl ester/tryptamine and 2-oxoaldehydes have been developed and successfully utilized for the total synthesis of Merinacarboline (A and B), Eudistomin Y1, Pityriacitrin B, Pityriacitrin, Fascaplysin and analogues.

Synthesis of 6-Substituted 3,5-diaryl-1,2,4-triazines as Potential Herbicidal Agents

Konno, Shoetsu,Osawa, Noriko,Yamanaka, Hiroshi,Sanemitsu, Yuzuru,Kawamura, Shinichi,Sakaki, Masaharu

, p. 838 - 842 (2007/10/02)

A variety of 6-substituted 3,5-diaryl-1,2,4-triazines were synthesized.These diaryltriazines, which incorporate a triazine nucleus substituted by two aryl moietes, comprise a new class of bleaching herbicides.The structure-activity relationships were prov

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