194930-03-5

• 

• Basic information

  1. Product Name: NAP 226-90-d6
  2. Synonyms: (S)-3-[[1-(Dimethyl-d6)amino)]ethyl]phenol;3-[[(1S)-1-(Dimethyl-d6)amino]ethyl]phenol;NAP 226-90-d6;3-[1-[Di(methyl-d3)amino]ethyl]phenol;N,N-Dimethyl-d6-N-[1-(3’-hydroxyphenyl)ethyl]amine;ZNS 114-666-d6
  3. CAS NO:194930-03-5
  4. Molecular Formula: C10H15NO
  5. Molecular Weight: 165.2322
  6. EINECS: N/A
  7. Product Categories: Intermediates & Fine Chemicals;Isotope Labeled Compounds;Metabolites & Impurities;Pharmaceuticals;Isotope Labelled Compounds;Isotope Labelled Compounds, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
  8. Mol File: 194930-03-5.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: 111-114°C
  2. Boiling Point: 241.337°C at 760 mmHg
  3. Flash Point: 97.243°C
  4. Appearance: /
  5. Density: 1.059g/cm³
  6. Vapor Pressure: 0.023mmHg at 25°C
  7. Refractive Index: 1.539
  8. Storage Temp.: Refrigerator
  9. Solubility: Chloroform, Dichloromethane, Methanol
  10. CAS DataBase Reference: NAP 226-90-d6(CAS DataBase Reference)
  11. NIST Chemistry Reference: NAP 226-90-d6(194930-03-5)
  12. EPA Substance Registry System: NAP 226-90-d6(194930-03-5)

• 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: 194930-03-5(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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194930-03-5 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 194930-03-5 differently. You can refer to the following data:
1. A labelled metabolite of Rivastigmine, a brain selective acetylcholinesterase inhibitor
2. An active (major) metabolite of Rivastigmine.

Check Digit Verification of cas no

The CAS Registry Mumber 194930-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,9,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 194930-03:
(8*1)+(7*9)+(6*4)+(5*9)+(4*3)+(3*0)+(2*0)+(1*3)=155
155 % 10 = 5
So 194930-03-5 is a valid CAS Registry Number.

InChI:InChI=1/C10H15NO/c1-8(11(2)3)9-5-4-6-10(12)7-9/h4-8,12H,1-3H3/i2D3,3D3

194930-03-5SDS

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	3-[1-[Di(methyl-d3)amino]ethyl]phenol

1.2 Other means of identification

Product number	-
Other names	3-[1-[bis(trideuteriomethyl)amino]ethyl]phenol

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:194930-03-5 SDS

194930-03-5Upstream product

• 14802-36-9 dimethylamine-D₆ 
• 121-71-1 3-Hydroxyacetophenone 

194930-03-5Downstream Products

194930-03-5Relevant articles and documents

Synthesis of tritium, deuterium and carbon-14 labeled (S)-N-ethyl-N-methyl-3-[1-(dimethylamino)ethyl]carbamic acid, phenyl ester, (L)-2,3-dihydroxybutanedioic acid salt (SDZ ENA 713 hta), an investigational drug for the treatment of Alzheimer's disease

Ciszewska, Grazyna,Pfefferkorn, Heidi,Tang,Jones, Lawrence,Tarapata, Richard,Sunay, Ustun B.

, p. 651 - 668 (1997)

(S)-(-)-N-Ethyl-N-methyl-3-[1-(dimethylamino)ethyl] carbamic acid, phenyl-2-3H-ester, (L)-2,3-dihydroxybutanedioic acid salt was synthesized via directed ortho-metallation methodology. (S)-(-)-N-Ethyl-N-methyl-3-[1-(di-(2H3)-methylamino)ethyl]carbamic acid, phenyl ester, (L)-2,3-dihydroxybutanedioic acid salt was synthesized from 3-hydroxyacetophenone. The molecule was resolved by classical diastereomeric salt formation and fractional crystallization. The carbon-14 analog, (S)-(-)-N-ethyl-N-methyl-3-[1-(dimethylamino)ethyl-1-(14C)]carbamic acid, phenyl ester, (L)-2,3-dihydroxybutanedioic acid salt was constructed starting from 3-iodoanisole and featured the enantioselective reduction of a methoxylamine intermediate.

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