Cas 500199-22-4,(Z)-2-((2S,3R,4S,5R,6R)-6-Aminomethyl-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-3-(4-methoxy-phenyl)-acrylic acid methyl ester

500199-22-4

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Basic information

Product Name: (Z)-2-((2S,3R,4S,5R,6R)-6-Aminomethyl-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-3-(4-methoxy-phenyl)-acrylic acid methyl ester
Synonyms:
CAS NO:500199-22-4
Molecular Formula:
Molecular Weight: 369.372
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: (Z)-2-((2S,3R,4S,5R,6R)-6-Aminomethyl-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-3-(4-methoxy-phenyl)-acrylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-((2S,3R,4S,5R,6R)-6-Aminomethyl-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-3-(4-methoxy-phenyl)-acrylic acid methyl ester(500199-22-4)
EPA Substance Registry System: (Z)-2-((2S,3R,4S,5R,6R)-6-Aminomethyl-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-3-(4-methoxy-phenyl)-acrylic acid methyl ester(500199-22-4)

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: 500199-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 500199-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,1,9 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 500199-22:
(8*5)+(7*0)+(6*0)+(5*1)+(4*9)+(3*9)+(2*2)+(1*2)=114
114 % 10 = 4
So 500199-22-4 is a valid CAS Registry Number.

500199-22-4Upstream product

295797-74-9 methyl (Z)-2-(6'-azido-β-D-galactopyranosyloxy)-3-p-hydroxyphenylacrylate

500199-22-4Downstream Products

500199-22-4Relevant academic research and scientific papers

Visualization of the precise structure recognition of leaf-opening substance by using biologically inactive probe compounds: Fluorescence studies of nyctinasty in legumes 2

Sugimoto, Takanori,Yamamura, Shosuke,Ueda, Minoru

, p. 1118 - 1119 (2002)

Intimate correlation between bioactivity and binding activity was shown using biologically active and inactive fluorescence-labeled probe compounds for nyctinasty. This results suggested the existence of a receptor which recognizes the aglycon of a leaf-o

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