Cas 475175-24-7,B10H10C(CH3)C(CH2)3OPO3(C6H4Cl)(CH2)3CB10H10C(CH2)3OH

475175-24-7

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Basic information

Product Name: B₁₀H₁₀C(CH₃)C(CH₂)3OPO₃(C₆H₄Cl)(CH₂)3CB₁₀H₁₀C(CH₂)3OH
Synonyms: B₁₀H₁₀C(CH₃)C(CH₂)3OPO₃(C₆H₄Cl)(CH₂)3CB₁₀H₁₀C(CH₂)3OH
CAS NO:475175-24-7
Molecular Formula:
Molecular Weight: 649.229
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: B₁₀H₁₀C(CH₃)C(CH₂)3OPO₃(C₆H₄Cl)(CH₂)3CB₁₀H₁₀C(CH₂)3OH(CAS DataBase Reference)
NIST Chemistry Reference: B₁₀H₁₀C(CH₃)C(CH₂)3OPO₃(C₆H₄Cl)(CH₂)3CB₁₀H₁₀C(CH₂)3OH(475175-24-7)
EPA Substance Registry System: B₁₀H₁₀C(CH₃)C(CH₂)3OPO₃(C₆H₄Cl)(CH₂)3CB₁₀H₁₀C(CH₂)3OH(475175-24-7)

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: 475175-24-7(Hazardous Substances Data)

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475175-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 475175-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,1,7 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 475175-24:
(8*4)+(7*7)+(6*5)+(5*1)+(4*7)+(3*5)+(2*2)+(1*4)=167
167 % 10 = 7
So 475175-24-7 is a valid CAS Registry Number.

475175-24-7Upstream product

67-56-1 methanol

475175-24-7Downstream Products

475175-27-0 B₁₀H₁₀C(CH₃)C(CH₂)3OPO₃(C₆H₄Cl)(CH₂)3CB₁₀H₁₀C(CH₂)2COOH

475175-24-7Relevant academic research and scientific papers

Synthesis of a porphyrin-labelled carboranyl phosphate diester: A potential new drug for boron neutron capture therapy of cancer

Maderna, Andreas,Huertas, Ramon,Hawthorne, M. Frederick,Luguya, Raymond,Graca,Vicente

, p. 1784 - 1785 (2007/10/03)

A boron-rich, water-soluble porphyrin conjugate was synthesized by coupling of two carboranyl alcohols with 2-chlorophenoxyphosphorus dichloride, followed by conjugation to an amine-functionalized tetraphenyl-porphyrin via an amide linkage.

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