107018-37-1

• 

• Basic information

  1. Product Name: Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)- (9CI)
  2. Synonyms: Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)- (9CI);4-(2,2,2-trifluoro-1-hydroxyethyl)benzonitrile;Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)-
  3. CAS NO:107018-37-1
  4. Molecular Formula: C₉H₆F₃NO
  5. Molecular Weight: 201.1452496
  6. EINECS: N/A
  7. Product Categories: ACETYLHALIDE
  8. Mol File: 107018-37-1.mol
  9. Article Data: 15

• 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.: 2-8°C
  8. Solubility: N/A
  9. CAS DataBase Reference: Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)- (9CI)(107018-37-1)
  11. EPA Substance Registry System: Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)- (9CI)(107018-37-1)

• 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: 107018-37-1(Hazardous Substances Data)

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• SDS
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107018-37-1 Usage

General Description

Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)- (9CI) is a chemical compound with the molecular formula C9H6F3NO. It is a derivative of benzonitrile, which is a colorless liquid with a faint almond-like odor. The addition of a 2,2,2-trifluoro-1-hydroxyethyl group to the benzonitrile molecule changes its chemical and physical properties, potentially affecting its reactivity and solubility. Benzonitrile, 4-(2,2,2-trifluoro-1-hydroxyethyl)- (9CI) may have potential applications in the pharmaceutical or chemical industries, but further research is needed to fully understand its properties and potential uses. However, its specific uses, hazards, and regulatory status should be thoroughly investigated before handling or using this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 107018-37-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,1 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107018-37:
(8*1)+(7*0)+(6*7)+(5*0)+(4*1)+(3*8)+(2*3)+(1*7)=91
91 % 10 = 1
So 107018-37-1 is a valid CAS Registry Number.

107018-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-(2,2,2-Trifluoro-1-hydroxyethyl)benzonitrile

1.2 Other means of identification

Product number	-
Other names	1-(4-cyanophenyl)-2,2,2-trifluoroethanol

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:107018-37-1 SDS

107018-37-1Upstream product

• 844-40-6 diphenylmethanol trifluoroacetate 
• 3058-39-7 4-iodobenzonitrile 
• 105-07-7 4-cyanobenzaldehyde 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 2314-97-8 iodotrifluoromethane 
• 75-63-8 Bromotrifluoromethane 

107018-37-1Downstream Products

• 1135312-09-2 (R)-2,2,2-trifluoro-1-(4'-cyanophenyl)ethanol 
• 1135311-95-3 (S)-2,2,2-trifluoro-1-(4'-cyanophenyl)ethyl isobutyrate 
• 1135312-30-9 2,2,2-trifluoro-1-(4'-cyanophenyl)ethyl isobutyrate 
• 193954-48-2 4-(2,2,2-trifluoro-1,1-dihydroxyethyl)benzonitrile 
• 23516-85-0 4-(2,2,2-trifluoroacetyl)benzonitrile 

107018-37-1Relevant articles and documents

Visible light-promoted umpolung coupling of aryl tri-/difluoroethanones with 2-alkenylpyridines

Xu, Xiao,Min, Qing-Qiang,Li, Na,Liu, Feng

, p. 11017 - 11020 (2018)

Tertiary alcohols bearing a trifluoromethyl group are of considerable medicinal interest. Using an umpolung strategy, we herein report the first intermolecular reductive cross-coupling of aryl tri-/difluoroethanones with 2-alkenylpyridines with the aid of a Br?nsted acid catalyst upon visible-light irradiation. This metal-free reaction is operationally simple and performed at ambient temperature, allowing access to desired tertiary alcohols with tri-/difluoromethyl groups in moderate to excellent yields. The commercially available and easily handled Hantzsch ester effectively serves as an electron donor, as well as a hydrogen atom source.

One-Pot and Reducible-Functional-Group-Tolerant Synthesis of α-Aryl- and α-Heteroaryl-α-Trifluoromethyl Alcohols via Tandem Trifluoroacetylation and MPV Type Reduction

Funabiki, Kazumasa,Hayakawa, Ayaka,Kani, Ryunosuke,Inuzuka, Toshiyasu,Kubota, Yashuhiro

, p. 5978 - 5984 (2019)

We have developed a new one-pot synthesis of α-aryl- and α-heteroaryl-α-trifluoromethyl alcohols carrying not only arenes with electron-withdrawing groups but also electron-deficient nitrogen-containing heteroarenes, which are of increasing interest becau

Nucleophilic trifluoromethylation using trifluoromethyl iodide. A new and simple alternative for the trifluoromethylation of aldehydes and ketones

Ait-Mohand, Samia,Takechi, Naoto,Medebielle, Maurice,Dolbier Jr., William R.

, p. 4271 - 4273 (2001)

(Matrix Presented) A novel method for nucleophilic trifluoromethylation of aldehydes and ketones, based on photoinduced reduction of trifluoromethyl iodide by tetrakis(dimethylamino)ethylene (TDAE), is presented.

FUROSEMIDE ANALOGUES AND COMPOSITIONS AND USES THEREOF FOR TREATMENT OF ALZHEIMER'S DISEASE

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Paragraph 0056; 0059; 00117-00118, (2021/01/23)

The present application provides furosemide analogues of the general formula Z having activity as anti-Aβ aggregation agents and/or as inhibitors of Aβ induced neuroinflammation. Formula Z These compounds are useful in preventing, delaying and/or treating Alzheimer's Disease. Accordingly, the present application further provides pharmaceutical compositions and method for preventing, delaying and/or treating Alzheimer's Disease.

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