Cas 630125-70-1,Benzenamine, 4-[(2-chloro-4-pyridinyl)oxy]-

630125-70-1

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Basic information

Product Name: Benzenamine, 4-[(2-chloro-4-pyridinyl)oxy]-
Synonyms:
CAS NO:630125-70-1
Molecular Formula: C11H9ClN2O
Molecular Weight: 220.658
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: Benzenamine, 4-[(2-chloro-4-pyridinyl)oxy]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenamine, 4-[(2-chloro-4-pyridinyl)oxy]-(630125-70-1)
EPA Substance Registry System: Benzenamine, 4-[(2-chloro-4-pyridinyl)oxy]-(630125-70-1)

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: 630125-70-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 630125-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,0,1,2 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 630125-70:
(8*6)+(7*3)+(6*0)+(5*1)+(4*2)+(3*5)+(2*7)+(1*0)=111
111 % 10 = 1
So 630125-70-1 is a valid CAS Registry Number.

630125-70-1Upstream product

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630125-70-1Relevant academic research and scientific papers

URACIL DERIVATIVES AS MER-AXL INHIBITORS

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, (2019/11/19)

The invention relates generally to compounds that are Mer-Axl inhibitors, pharmaceutical compositions containing said compounds and methods of treating proliferative disorders and disorders of dysregulated apoptosis, such as cancer, utilizing the compounds of the invention.

AGRICULTURAL CHEMICALS

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Page/Page column 59; 104, (2019/08/08)

The present invention relates to picolinic acid derivatives that are useful in treating fungal diseases ofplants.

NOVEL SUBSTITUTED PYRIDINYLOXY AND PYRIMIDINYLOXY AMIDES USEFUL AS INHIBITORS OF PROTEIN KINASES

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Page/Page column 25, (2010/11/27)

The present invention relates to compounds and methods useful as inhibitors of protein kinases, including B-Raf and several receptor tyrosine and cytoplasmic tyrosine kinases. The present invention is directed to new substituted pyrimidinyloxy urea compounds of Formulas II, III and IV and compositions and their application as pharmaceuticals for the treatment of disease. Methods of modulating of protein kinase activity in a human or animal subject are also provided for the treatment diseases such as cancers.

PYRIMIDINE DERIVATIVES FOR TREATMENT OF HYPERPROLIFERATIVE DISORDERS

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Page/Page column 49, (2010/11/23)

Pyrimidine derivatives of formula (I), pharmaceutical compositions containing these compounds, and methods of using these compounds in treatment of hyperproliferative diseases such as cancer are disclosed and claimed.

PYRIMIDINE DERIVATIVES FOR TREATMENT OF HYPERPROLIFERATIVE DISORDERS

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Page/Page column 64, (2008/06/13)

Pyrimidine derivatives of formula (I) in which J and Y represent aromatic or heteroaromatic rings; R2, G, G', and G" represent substituent groups and R2a represents H or halogen; L represents a linking group; and M represents CH or N. Pharmaceutical compositions containing these compounds, and methods of using these compounds in treatment of hyperproliferative diseases such as cancer are also disclosed and claimed.

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