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2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1345985-97-8

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1345985-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1345985-97-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,9,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1345985-97:
(9*1)+(8*3)+(7*4)+(6*5)+(5*9)+(4*8)+(3*5)+(2*9)+(1*7)=208
208 % 10 = 8
So 1345985-97-8 is a valid CAS Registry Number.

1345985-97-8Relevant academic research and scientific papers

Identification of novel 2-((1-(benzyl(2-hydroxy-2-phenylethyl)amino)-1-oxo- 3-phenylpropan-2-yl)carbamoyl)benzoic acid analogues as BMP-2 stimulators

Balaramnavar, Vishal M.,Khan, Imran A.,Siddiqui, Jawed Akhtar,Khan, Mohd Parvez,Chakravarti, Bandana,Sharan, Kunal,Swarnkar, Gaurav,Rastogi, Namrata,Siddiqui,Mishra, Durga Prasad,Chattopadhyay, Naibedya,Saxena, Anil K.

, p. 8248 - 8259 (2013/01/15)

The synthesis and SAR studies of 10 new chemical entities (NCEs) that have shown BMP-2 stimulation and osteoblast differentiation are reported. Among these, 2-((1-(benzyl(2-hydroxy-2-phenylethyl)amino)-1-oxo-3-phenylpropan-2-yl) carbamoyl)benzoic acid (11) was the most effective while its analogue 13 also showed good activity in inducing osteoblast BMP-2 production. Compound 11 induced osteoblast differentiation in vitro, and this effect was abrogated by a physiological BMP-2 inhibitor, noggin. It also exhibited dose dependent increase in nascent bone formation (2.16- and 3.12-fold more than the control at 1 and 5 mg/kg dose, respectively) at the fracture site in rats. At the maximum osteogenic concentration, compound 11 significantly inhibited osteoblastic proteosomal activity. This compound was safe, as it had no effect on BMP synthesis in cardiovascular tissue.

Synthesis and 2D QSAR of O-sulphonated β-aminols derivatives as novel antifungal and antibacterial agents

Saxena, Anil K.,Sharma, Sugandha,Pandey, Atindra K.,Shukla, Praveen K.

, p. 6476 - 6481 (2011/11/29)

Synthesis of a series of b-aminol derivatives using regioselective opening reaction catalyzed by SiO2 (60-120 mesh) and O-sulphonation in THF-KOH system, comprising tert-butoxycarbonyl at secondary nitrogen and evaluate for various stains of bacteria and fungi. SAR study of synthesized compound using backward regression analysis.

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