Basic information

Product Name: Octanoic acid, 3-ethyl-, ethyl ester
Synonyms:
CAS NO:64318-63-4
Molecular Formula: C12H24O2
Molecular Weight: 200.321
EINECS: N/A
Product Categories: N/A

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: Octanoic acid, 3-ethyl-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Octanoic acid, 3-ethyl-, ethyl ester(64318-63-4)
EPA Substance Registry System: Octanoic acid, 3-ethyl-, ethyl ester(64318-63-4)

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: 64318-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 64318-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,1 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64318-63:
(7*6)+(6*4)+(5*3)+(4*1)+(3*8)+(2*6)+(1*3)=124
124 % 10 = 4
So 64318-63-4 is a valid CAS Registry Number.

64318-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	(-)(S)-3-pentyl-valeric acid ethyl ester

1.2 Other means of identification

Product number	-
Other names	(-)(S)-3-Pentyl-valeriansaeure-aethylester

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:64318-63-4 SDS

64318-63-4Upstream product

64318-63-4Downstream Products

64318-63-4Relevant academic research and scientific papers

HOMOLOGATION OF N-ALKANES USING DIAZOESTERS AND RHODIUM(III)PORPHYRINS. ENHANCED ATTACK ON PRIMARY C-H BONDS.

Callot, H.J.,Metz, F.

, p. 4321 - 4324 (2007/10/02)

Carbethoxycarbene, from ethyl diazoacetate and rhodium(III)porphyrins, inserted into methyl C-H bonds of n-alkenes (C6 to C12) with yields up to 20-25 percent corresponding to a large increase of the primary/secondary selectivity.

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