Cas 77407-45-5,4-Hydroxy-2-methylene-4-phenyl-pentanoic acid (2-methoxy-phenyl)-amide

77407-45-5

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Basic information

Product Name: 4-Hydroxy-2-methylene-4-phenyl-pentanoic acid (2-methoxy-phenyl)-amide
Synonyms: 4-Hydroxy-2-methylene-4-phenyl-pentanoic acid (2-methoxy-phenyl)-amide
CAS NO:77407-45-5
Molecular Formula:
Molecular Weight: 311.381
EINECS: N/A
Product Categories: N/A
Mol File: 77407-45-5.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: 4-Hydroxy-2-methylene-4-phenyl-pentanoic acid (2-methoxy-phenyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: 4-Hydroxy-2-methylene-4-phenyl-pentanoic acid (2-methoxy-phenyl)-amide(77407-45-5)
EPA Substance Registry System: 4-Hydroxy-2-methylene-4-phenyl-pentanoic acid (2-methoxy-phenyl)-amide(77407-45-5)

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: 77407-45-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 77407-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77407-45:
(7*7)+(6*7)+(5*4)+(4*0)+(3*7)+(2*4)+(1*5)=145
145 % 10 = 5
So 77407-45-5 is a valid CAS Registry Number.

77407-45-5Upstream product

77407-45-5Downstream Products

29043-98-9 γ-methyl-α-methylene-γ-phenyl-γ-butyrolactone

77407-45-5Relevant articles and documents

DIANION OF N-(o-METHOXYPHENYL)-2-METHYLPROPENAMIDE: A NEW REAGENT FOR THE CONVENIENT SYNTHESIS OF α-METHYLENE-γ-BUTYROLACTONES FROM CARBONYL COMPOUNDS

Tanaka, Kazuhiko,Nozaki, Yoshihito,Tamura, Norikazu,Tanikaga, Rikuhei,Kaji, Aritsune

, p. 1567 - 1568 (1980)

Dianion of N-(o-methoxyphenyl)-2-methylpropenamide was successfully generated on treatment of the amide with t-BuOK-BuLi at -78 degC in THF and utilized as the key reagent for the synthesis of γ-substituted α-methylene-γ-butyrolactones.

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