Cas 1595164-24-1,nonane-5,5-diylbis(2-methyl-4,1-phenylene) bis(sulfamate)

1595164-24-1

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Basic information

Product Name: nonane-5,5-diylbis(2-methyl-4,1-phenylene) bis(sulfamate)
Synonyms: nonane-5,5-diylbis(2-methyl-4,1-phenylene) bis(sulfamate)
CAS NO:1595164-24-1
Molecular Formula:
Molecular Weight: 498.665
EINECS: N/A
Product Categories: N/A
Mol File: 1595164-24-1.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: nonane-5,5-diylbis(2-methyl-4,1-phenylene) bis(sulfamate)(CAS DataBase Reference)
NIST Chemistry Reference: nonane-5,5-diylbis(2-methyl-4,1-phenylene) bis(sulfamate)(1595164-24-1)
EPA Substance Registry System: nonane-5,5-diylbis(2-methyl-4,1-phenylene) bis(sulfamate)(1595164-24-1)

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: 1595164-24-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1595164-24-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,5,1,6 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1595164-24:
(9*1)+(8*5)+(7*9)+(6*5)+(5*1)+(4*6)+(3*4)+(2*2)+(1*4)=191
191 % 10 = 1
So 1595164-24-1 is a valid CAS Registry Number.

1595164-24-1Upstream product

57100-73-9 4,4'-(nonane-5,5-diyl)bis(2-methylphenol)

1595164-24-1Downstream Products

1595164-24-1Relevant articles and documents

Design and synthesis of silicon-containing steroid sulfatase inhibitors possessing pro-estrogen antagonistic character

Kajita, Daisuke,Nakamura, Masaharu,Matsumoto, Yotaro,Makishima, Makoto,Hashimoto, Yuichi

, p. 2244 - 2252 (2014)

Steroid sulfatase (STS) is a potential target for treatment of postmenopausal hormone-dependent breast cancer. Several steroidal STS inhibitors have been reported, but steroidal compounds are difficult to optimize and may interact with other targets. On t

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