78263-38-4

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Basic information

Product Name: 2-Propenal, 3,3-bis(methylthio)-
Synonyms:
CAS NO:78263-38-4
Molecular Formula: C5H8OS2
Molecular Weight: 148.25
EINECS: N/A
Product Categories: N/A
Mol File: 78263-38-4.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-Propenal, 3,3-bis(methylthio)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Propenal, 3,3-bis(methylthio)-(78263-38-4)
EPA Substance Registry System: 2-Propenal, 3,3-bis(methylthio)-(78263-38-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 78263-38-4(Hazardous Substances Data)

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78263-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78263-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,2,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78263-38:
(7*7)+(6*8)+(5*2)+(4*6)+(3*3)+(2*3)+(1*8)=154
154 % 10 = 4
So 78263-38-4 is a valid CAS Registry Number.

78263-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-nitro-3-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)benzoic acid

1.2 Other means of identification

Product number	-
Other names	-

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).

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78263-38-4Relevant articles and documents

Formation of acetaldehyde enolate from vinyl acetate and its reaction with aromatic and heterocyclic aldehydes: An efficient synthesis of enals and polyenals

Mahata,Barun,Ila,Junjappa

, p. 1345 - 1347 (2007/10/03)

Two carbon homologation of aromatic and heterocyclic aldehydes is achieved by reacting them with acetaldehyde enolate anion generated in situ by cleaving vinyl acetate in the presence of barium hydroxide.

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