10242-52-1

• 

• Basic information

  1. Product Name: Acetonitrile, [(1-methyl-2-phenylethyl)nitrosoamino]-
  2. Synonyms:
  3. CAS NO:10242-52-1
  4. Molecular Formula: C11H13N3O
  5. Molecular Weight: 203.244
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 10242-52-1.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Acetonitrile, [(1-methyl-2-phenylethyl)nitrosoamino]-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Acetonitrile, [(1-methyl-2-phenylethyl)nitrosoamino]-(10242-52-1)
  11. EPA Substance Registry System: Acetonitrile, [(1-methyl-2-phenylethyl)nitrosoamino]-(10242-52-1)

• 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: 10242-52-1(Hazardous Substances Data)

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• SDS
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• Downstream Products
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10242-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10242-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,4 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10242-52:
(7*1)+(6*0)+(5*2)+(4*4)+(3*2)+(2*5)+(1*2)=51
51 % 10 = 1
So 10242-52-1 is a valid CAS Registry Number.

10242-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	N-(cyanomethyl)-N-(1-phenylpropan-2-yl)nitrous amide

1.2 Other means of identification

Product number	-
Other names	Acetonitrile,[(1-methyl-2-phenylethyl)nitrosoamino]

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:10242-52-1 SDS

10242-52-1Upstream product

• 30825-14-0 (1-methyl-2-phenylethylamino)acetonitrile 
• 22293-47-6 3-(α-methylphenethyl)sydnone imine 
• 3441-64-3 3-(α-methylphenethyl)sydnone imine hydrochloride 

10242-52-1Downstream Products

• 78915-45-4 N₆-Ethoxycarbonylbenzyl-3-phenylisopropylsydnonimine 
• 117038-04-7 N₆-<4-(2-Diethylaminoethoxycarbonyl)phenylcarbamoyl>-3-phenylisopropylsydnone imine 
• 3441-64-3 3-(α-methylphenethyl)sydnone imine hydrochloride 
• 67629-54-3 N₆-(4-Tolyl-carbamoyl)-3-phenylisopropylsydnone imine 
• 117015-64-2 N₆-(2-Tolyl-carbamoyl)-3-phenylisopropylsydnone imine 
• 78915-39-6 N₆-Ethoxycarbonylphenyl-3-phenylisopropylsydnonimine 
• 117015-71-1 N₆-(4-Aminophenylcarbamoyl)-3-phenylisopropylsydnone imine dihydrochloride 
• 78915-46-5 5-[3-(4-carboxy-benzyl)-ureido]-3-(1-methyl-2-phenyl-ethyl)-[1,2,3]oxadiazolium betaine 
• 78915-40-9 5-[3-(4-carboxy-phenyl)-ureido]-3-(1-methyl-2-phenyl-ethyl)-[1,2,3]oxadiazolium betaine 

10242-52-1Relevant articles and documents

Synthesis and characterization of hydroxylated mesocarb metabolites for doping control

Vahermo, Mikko,Suominen, Tina,Leinonen, Antti,Yli-Kauhaluoma, Jari

experimental part, p. 201 - 209 (2009/05/09)

The synthesis and method of analysis of hydroxylated mesocarb metabolites are described. Six potential hydroxylated mesocarb metabolites were prepared, characterized, and compared with the mesocarb metabolites synthesized enzymatically in vitro using human liver proteins and also compared with metabolites extracted from human urine after oral administration of mesocarb. p-Hydroxymesocarb was the most prevalent metabolite (conjugated and non-conjugated) observed. With respect to doping analysis, synthesis of p-hydroxymesocarb, the main urinary metabolite of mesocarb, and its availability as a reference material is important.

A SYDNONEIMINE BASE

Ogorodnikova, V. V.,Kholodov, L. E.,Yashunskii, V. G.

, p. 598 - 602 (2007/10/02)

It was shown by means of the UV spectra that a sydnoneimine base is formed from 3-cyclohexyl sydnoneimine hydrochloride by the action of an equivalent amount of sodium hydroxide in solutions of absolute alcohols.The sydnoneimine base is also formed in the case of solvolysis of N6-trimethylsilyl-3-cyclohexylsydnoneimine in methanol.The sydnoneimine base in solutions exists in equilibrium with the chain isomer, viz., the nitrile.The fraction of the cyclic isomer increases as the electron-donor properties of the substituent in the 3 position become more pronounced.

BIOTRANSFORMATION OF SYDNOCARB IN THE RAT

Kholodov, L. E.

, p. 477 - 481 (2007/10/02)

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