Cas 1236308-69-2,methyl (E,S)-3-methyl-2-[4-(4-methylbenzoyloxy)-3-ethoxybenzylideneamino]butyrate

1236308-69-2

Post Buying Request

Basic information

Product Name: methyl (E,S)-3-methyl-2-[4-(4-methylbenzoyloxy)-3-ethoxybenzylideneamino]butyrate
Synonyms:
CAS NO:1236308-69-2
Molecular Formula:
Molecular Weight: 397.471
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: methyl (E,S)-3-methyl-2-[4-(4-methylbenzoyloxy)-3-ethoxybenzylideneamino]butyrate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (E,S)-3-methyl-2-[4-(4-methylbenzoyloxy)-3-ethoxybenzylideneamino]butyrate(1236308-69-2)
EPA Substance Registry System: methyl (E,S)-3-methyl-2-[4-(4-methylbenzoyloxy)-3-ethoxybenzylideneamino]butyrate(1236308-69-2)

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: 1236308-69-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1236308-69-2 Suppliers

Recommended suppliers

1236308-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1236308-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,3,0 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1236308-69:
(9*1)+(8*2)+(7*3)+(6*6)+(5*3)+(4*0)+(3*8)+(2*6)+(1*9)=142
142 % 10 = 2
So 1236308-69-2 is a valid CAS Registry Number.

1236308-69-2Upstream product

1236308-69-2Downstream Products

1236308-69-2Relevant academic research and scientific papers

Synthesis of chiral azomethines starting from L-valine methyl ester hydrochloride and substituted benzaldehydes of vanillin series

Dikusar,Potkin,Zhukovskaya

experimental part, p. 644 - 648 (2010/10/04)

A preparative method of synthesis of chiral azomethines was developed consisting in the reaction of L-valine methyl ester hydrochloride reaction with substituted benzaldehydes of vanillin series. Pleiades Publishing, Ltd., 2010.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 1236308-69-2