Cas 118450-15-0,3-(2-hydroxyphenyl)-1-thiocarbamyl-5-thiosemicarbazide-2-pyrazoline

118450-15-0

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Basic information

Product Name: 3-(2-hydroxyphenyl)-1-thiocarbamyl-5-thiosemicarbazide-2-pyrazoline
Synonyms: 3-(2-hydroxyphenyl)-1-thiocarbamyl-5-thiosemicarbazide-2-pyrazoline
CAS NO:118450-15-0
Molecular Formula:
Molecular Weight: 310.404
EINECS: N/A
Product Categories: N/A
Mol File: 118450-15-0.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: 3-(2-hydroxyphenyl)-1-thiocarbamyl-5-thiosemicarbazide-2-pyrazoline(CAS DataBase Reference)
NIST Chemistry Reference: 3-(2-hydroxyphenyl)-1-thiocarbamyl-5-thiosemicarbazide-2-pyrazoline(118450-15-0)
EPA Substance Registry System: 3-(2-hydroxyphenyl)-1-thiocarbamyl-5-thiosemicarbazide-2-pyrazoline(118450-15-0)

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: 118450-15-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118450-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,4,5 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118450-15:
(8*1)+(7*1)+(6*8)+(5*4)+(4*5)+(3*0)+(2*1)+(1*5)=110
110 % 10 = 0
So 118450-15-0 is a valid CAS Registry Number.

118450-15-0Upstream product

118450-15-0Downstream Products

34810-67-8 2-(1H-pyrazol-3-yl)phenol

118450-15-0Relevant articles and documents

BENZO-γ-PYRONES. PART XIII. REACTION OF CHROMONE AND ITS METHYL DERIVATIVES WITH THIOSEMICARBAZIDE

Maib, Piotr,Jerzmanowska, Zofia

, p. 111 - 122 (2007/10/02)

The reaction of chromone and its C-2 and C-3 substituted methyl derivatives was studied.New compounds in the systems of 2-pyrazoline (3, 14), 1,3-butanedione (9), pyrazole (4, 10, 11, 15) and chromone (7) were obtained.Methyl groups at C-2 and C-3 position desactivate the chromone system towards thiosemicarbazide.

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