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N-(t-Butoxycarbonyl)-3-(2-cyclohexylethyl)-L-histidine methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111102-67-1

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111102-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111102-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,0 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111102-67:
(8*1)+(7*1)+(6*1)+(5*1)+(4*0)+(3*2)+(2*6)+(1*7)=51
51 % 10 = 1
So 111102-67-1 is a valid CAS Registry Number.

111102-67-1Relevant academic research and scientific papers

Substrate-based design of the first class of angiotensin-converting enzyme-related carboxypeptidase (ACE2) inhibitors

Dales, Natalie A.,Gould, Alexandra E.,Brown, James A.,Calderwood, Emily F.,Guan, Bing,Minor, Charles A.,Gavin, James M.,Hales, Paul,Kaushik, Virendar K.,Stewart, Michael,Tummino, Peter J.,Vickers, Chad S.,Ocain, Timothy D.,Patane, Michael A.

, p. 11852 - 11853 (2007/10/03)

Angiotensin-converting enzyme-related carboxypeptidase (ACE2) is a recently identified zinc metalloprotease with carboxypeptidase activity that was identified using our genomics platform. We implemented a rational design approach to identify potent and se

Synthesis and Structure-Activity Relationships of a Novel Series of Non-Peptide Angiotensin II Receptor Binding Inhibitors Specific for the AT2 Subtype

Blankley, C. John,Hodges, John C.,Klutchko, Sylvester R.,Himmelsbach, Richard J.,Chucholowski, Alexander,et al.

, p. 3248 - 3260 (2007/10/02)

Structure-activity relationships are reported for a novel class of 4,5,6,7-tetrahydro-1H-imidazopyridine-6-carboxylic acid derivatives that displace 125I-labeled angiotensin II from a specific subset of angiotensin II (Ang II) binding sites in rat

Regiospecific Synthesis of 3-Substituted L-Histidines

Hodges, John C.

, p. 20 - 24 (2007/10/02)

3-Substituted L-histidine derivatives were prepared by a regiospecific alkylation of N,1-bis-Boc-L-histidine methyl ester with in situ-generated alkyl triflates, benzyl triflates, and benzyl mesylates.Subsequent acid hydrolysis of N-Boc and methyl ester p

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