121731-72-4

• 

• Basic information

  1. Product Name: Carbamic acid, (3-oxopropyl)-2-propenyl-, methyl ester (9CI)
  2. Synonyms: Carbamic acid, (3-oxopropyl)-2-propenyl-, methyl ester (9CI)
  3. CAS NO:121731-72-4
  4. Molecular Formula: C8H13NO3
  5. Molecular Weight: 0
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 121731-72-4.mol
  9. Article Data: 1

• 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: Carbamic acid, (3-oxopropyl)-2-propenyl-, methyl ester (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Carbamic acid, (3-oxopropyl)-2-propenyl-, methyl ester (9CI)(121731-72-4)
  11. EPA Substance Registry System: Carbamic acid, (3-oxopropyl)-2-propenyl-, methyl ester (9CI)(121731-72-4)

• 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: 121731-72-4(Hazardous Substances Data)

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121731-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121731-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,3 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121731-72:
(8*1)+(7*2)+(6*1)+(5*7)+(4*3)+(3*1)+(2*7)+(1*2)=94
94 % 10 = 4
So 121731-72-4 is a valid CAS Registry Number.

121731-72-4SDS

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	methyl N-allyl-N-(2-formylethyl)carbamate

1.2 Other means of identification

Product number	-
Other names	Allyl-(3-oxo-propyl)-carbamic acid methyl ester

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:121731-72-4 SDS

121731-72-4Upstream product

121731-72-4Downstream Products

121731-72-4Relevant articles and documents

Synthesis of the Chiral (8S)-7-Aza-1,3(E),9-decatriene System from Natural α-Amino Acids and Its Intramolecular Diels-Alder Reaction Directed toward Chiral trans-Hydroisoquinolones

Moriwake, Toshio,Hamano, Shin-ich,Saito, Seiki,Torii, Shigeru,Kashino, Setsuo

, p. 4114 - 4120 (2007/10/02)

L-Alanine and L-valine were converted into optically active 7-aza-1,3(E),9-decatrienes containing a (tert-butyldimethylsilyl)oxy group at C(2) and a methyl or isopropyl group at C(8).Intramolecular thermal cycloaddition reactions of these trienes gave optically active trans-nonahydro-6(2H)-isoquinolones.The relatively bulky isopropyl group at C(8) increased the trans selectivity in the ring closure.These results are in contrast with literature reports on ring closure of analogous aza trienes that lack the (tert-butyldimethylsilyl)oxy group at C(2), whichgive predominantly cis-fused rings.

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