Cas 1207104-63-9,tert-butyl (E)-2-({5-[furan-2-yl(propylamino)methyl]-1H-1,2,3,4-tetrazol-1-yl}methyl)-3-phenylprop-2-enoate

1207104-63-9

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Basic information

Product Name: tert-butyl (E)-2-({5-[furan-2-yl(propylamino)methyl]-1H-1,2,3,4-tetrazol-1-yl}methyl)-3-phenylprop-2-enoate
Synonyms: tert-butyl (E)-2-({5-[furan-2-yl(propylamino)methyl]-1H-1,2,3,4-tetrazol-1-yl}methyl)-3-phenylprop-2-enoate
CAS NO:1207104-63-9
Molecular Formula:
Molecular Weight: 423.515
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: tert-butyl (E)-2-({5-[furan-2-yl(propylamino)methyl]-1H-1,2,3,4-tetrazol-1-yl}methyl)-3-phenylprop-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (E)-2-({5-[furan-2-yl(propylamino)methyl]-1H-1,2,3,4-tetrazol-1-yl}methyl)-3-phenylprop-2-enoate(1207104-63-9)
EPA Substance Registry System: tert-butyl (E)-2-({5-[furan-2-yl(propylamino)methyl]-1H-1,2,3,4-tetrazol-1-yl}methyl)-3-phenylprop-2-enoate(1207104-63-9)

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: 1207104-63-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1207104-63-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,1,0 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1207104-63:
(9*1)+(8*2)+(7*0)+(6*7)+(5*1)+(4*0)+(3*4)+(2*6)+(1*3)=99
99 % 10 = 9
So 1207104-63-9 is a valid CAS Registry Number.

1207104-63-9Upstream product

1207104-63-9Downstream Products

1207105-52-9 C₁₉H₂₁N₅O₃

1207104-63-9Relevant academic research and scientific papers

Isonitriles from the Baylis-Hillman adducts of acrylates: viable precursor to tetrazolo-fused diazepinones via post-Ugi cyclization

Nayak, Maloy,Batra, Sanjay

, p. 510 - 516 (2010)

Stereocontrolled synthesis of substituted isonitriles from the Baylis-Hillman adducts of acrylates has been developed. Ugi reaction of these isonitriles with TMSN3, aliphatic amines, and aldehydes or ketone affords 1-substituted tetrazoles whic

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