Cas 530088-72-3,Carbamic acid, [(1S)-2-(octylamino)-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester

530088-72-3

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Basic information

Product Name: Carbamic acid, [(1S)-2-(octylamino)-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:530088-72-3
Molecular Formula: C23H38N2O4
Molecular Weight: 406.566
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: Carbamic acid, [(1S)-2-(octylamino)-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S)-2-(octylamino)-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(530088-72-3)
EPA Substance Registry System: Carbamic acid, [(1S)-2-(octylamino)-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(530088-72-3)

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: 530088-72-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 530088-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,0,0,8 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 530088-72:
(8*5)+(7*3)+(6*0)+(5*0)+(4*8)+(3*8)+(2*7)+(1*2)=133
133 % 10 = 3
So 530088-72-3 is a valid CAS Registry Number.

530088-72-3Upstream product

530088-72-3Downstream Products

530088-72-3Relevant academic research and scientific papers

Continuous in situ generation and reaction of phosgene in a microflow system

Fuse, Shinichiro,Tanabe, Nobutake,Takahashi, Takashi

, p. 12661 - 12663 (2012/01/03)

Continuous in situ generation of phosgene and its use in acid chloride formation in a microflow system were demonstrated. The acid chloride was subsequently coupled with an amine in high yield without severe epimerization. The Royal Society of Chemistry 2011.

Synthesis and pharmacological evaluation of second-generation phosphatidic acid derivatives as lysophosphatidic acid receptor ligands

Durgam, Gangadhar G.,Tsukahara, Ryoko,Makarova, Natalia,Walker, Michelle D.,Fujiwara, Yuko,Pigg, Kathryn R.,Baker, Daniel L.,Sardar, Vineet M.,Parrill, Abby L.,Tigyi, Gabor,Miller, Duane D.

, p. 633 - 640 (2007/10/03)

Short-chain phosphatidic acid derivatives, dioctanoyl glycerol pyrophosphate (DGPP 8:0, 1) and phosphatidic acid 8:0 (PA 8:0, 2), were previously identified as subtype-selective LPA1 and LPA3 receptor antagonists. Recently, we report

Synthesis and biological evaluation of novel cytotoxic phospholipids for prostate cancer

Gududuru, Veeresa,Hurh, Eunju,Durgam, Gangadhar G.,Hong, Seoung Soo,Sardar, Vineet M.,Xu, Huiping,Dalton, James T.,Miller, Duane D.

, p. 4919 - 4923 (2007/10/03)

A series of serine amide phosphates (SAPs) and serine amide alcohols (SAAs) were prepared and evaluated for their in vitro cytotoxicity against five human prostate cancer cell lines. The SAR and biological activity of the synthesized compounds is reported

Studies on scavenger receptor inhibitors. Part 1: Synthesis and structure-activity relationships of novel derivatives of sulfatides

Yoshiizumi, Kazuya,Nakajima, Fumio,Dobashi, Rika,Nishimura, Noriyasu,Ikeda, Shoji

, p. 2445 - 2460 (2007/10/03)

Scavenger receptors have been proven to be implicated in the formation of atherosclerotic lesions. A series of novel derivatives of sulfatides were synthesized, and their inhibitory activities against incorporation of DiI-acetyl-LDL into macrophages were

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