121985-97-5

• 

• Basic information

  1. Product Name: Benzeneacetonitrile, alpha-hydroxy-4-(1-methylethyl)-, (alphaR)- (9CI)
  2. Synonyms: Benzeneacetonitrile, alpha-hydroxy-4-(1-methylethyl)-, (alphaR)- (9CI)
  3. CAS NO:121985-97-5
  4. Molecular Formula: C₁₁H₁₃NO
  5. Molecular Weight: 175.22702
  6. EINECS: N/A
  7. Product Categories: ISOPROPYL
  8. Mol File: 121985-97-5.mol
  9. Article Data: 4

• 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.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Benzeneacetonitrile, alpha-hydroxy-4-(1-methylethyl)-, (alphaR)- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Benzeneacetonitrile, alpha-hydroxy-4-(1-methylethyl)-, (alphaR)- (9CI)(121985-97-5)
  11. EPA Substance Registry System: Benzeneacetonitrile, alpha-hydroxy-4-(1-methylethyl)-, (alphaR)- (9CI)(121985-97-5)

• 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: 121985-97-5(Hazardous Substances Data)

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• Article

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121985-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121985-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121985-97:
(8*1)+(7*2)+(6*1)+(5*9)+(4*8)+(3*5)+(2*9)+(1*7)=145
145 % 10 = 5
So 121985-97-5 is a valid CAS Registry Number.

121985-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-isopropyl-α-hydroxyphenylacetonitrile

1.2 Other means of identification

Product number	-
Other names	(R)-Hydroxy-(4-isopropyl-phenyl)-acetonitrile

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:121985-97-5 SDS

121985-97-5Upstream product

• 75-86-5 2-hydroxy-2-methylpropanenitrile 
• 122-03-2 (4-isopropylbenzaldehyde) 
• 7677-24-9 trimethylsilyl cyanide 
• 151-50-8 potassium cyanide 
• 74-90-8 hydrogen cyanide 

121985-97-5Downstream Products

121985-97-5Relevant articles and documents

Tertiary pentyl groups enhance salen titanium catalyst for highly enantioselective trimethylsilylcyanation of aldehydes

Liang, Sidney,Bu, Xiu R.

, p. 2702 - 2704 (2007/10/03)

tert-Pentyl groups are recognized to be highly effective steric groups that can enhance enantioselectivity of salen titanium complexes when they are used in asymmetrical cyanation of aromatic aldehydes. High ee (92-97%) has been obtained with several aldehyde substrates. Compared to its tert-butyl analogue, the tert-pentyl group has been found to improve enantioselectivity and in some cases quite dramatically.

Novel (R)-oxynitrilase sources for the synthesis of (R)-cyanohydrins in diisopropyl ether

Kiljunen, Eero,Kanerva, Liisa T.

, p. 1225 - 1234 (2007/10/03)

Apple, apricot, cherry and plum meal were prepared from the seeds or kernels of mature garden fruits. The preparations as well as almond meal were used as the source of (R)-oxynitrilase for the synthesis of aliphatic and aromatic cyanohydrins in diisoprop

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