Cas 104344-10-7,N<sup>α</sup>-<3-cyclohexyl-1(R)-ethoxycarbonylpropyl>-N<sup>ε</sup>-benzyloxycarbonyl-L-lysine tert-butyl ester

104344-10-7

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Basic information

Product Name: N^α-<3-cyclohexyl-1(R)-ethoxycarbonylpropyl>-N^ε-benzyloxycarbonyl-L-lysine tert-butyl ester
Synonyms:
CAS NO:104344-10-7
Molecular Formula:
Molecular Weight: 532.721
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: N^α-<3-cyclohexyl-1(R)-ethoxycarbonylpropyl>-N^ε-benzyloxycarbonyl-L-lysine tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N^α-<3-cyclohexyl-1(R)-ethoxycarbonylpropyl>-N^ε-benzyloxycarbonyl-L-lysine tert-butyl ester(104344-10-7)
EPA Substance Registry System: N^α-<3-cyclohexyl-1(R)-ethoxycarbonylpropyl>-N^ε-benzyloxycarbonyl-L-lysine tert-butyl ester(104344-10-7)

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: 104344-10-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104344-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,4 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104344-10:
(8*1)+(7*0)+(6*4)+(5*3)+(4*4)+(3*4)+(2*1)+(1*0)=77
77 % 10 = 7
So 104344-10-7 is a valid CAS Registry Number.

104344-10-7Upstream product

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104344-10-7Relevant academic research and scientific papers

Synthesis and angiotensin converting enzyme inhibitory activity of L-lysyl-N-substituted glycine derivatives

Saito,Matsui,Fukushima,Watanabe,Waga,Kajiwara,Shirota,Iijima,Kitabatake

, p. 1558 - 1561 (2007/10/02)

The synthesis and biological activity of novel L-lysyl-N-substituted glycine derivatives which exhibit in vitro and in vivo angiotensin converting enzyme (ACE) inhibition, are described. Particularly, N-[N(α)-(1-carboxy-3-phenylpropyl)-L-lysyl]-N-(4-pheny

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