Cas 188922-38-5,Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-2-ethyl-, 4-[[bis[[(phenylmethoxy)carbonyl]amino]methylene]amino]phenyl ester

188922-38-5

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Basic information

Product Name: Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-2-ethyl-, 4-[[bis[[(phenylmethoxy)carbonyl]amino]methylene]amino]phenyl ester
Synonyms:
CAS NO:188922-38-5
Molecular Formula: C34H40N4O8
Molecular Weight: 632.714
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: Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-2-ethyl-, 4-[[bis[[(phenylmethoxy)carbonyl]amino]methylene]amino]phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-2-ethyl-, 4-[[bis[[(phenylmethoxy)carbonyl]amino]methylene]amino]phenyl ester(188922-38-5)
EPA Substance Registry System: Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-2-ethyl-, 4-[[bis[[(phenylmethoxy)carbonyl]amino]methylene]amino]phenyl ester(188922-38-5)

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: 188922-38-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 188922-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,9,2 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 188922-38:
(8*1)+(7*8)+(6*8)+(5*9)+(4*2)+(3*2)+(2*3)+(1*8)=185
185 % 10 = 5
So 188922-38-5 is a valid CAS Registry Number.

188922-38-5Upstream product

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188922-38-5Relevant academic research and scientific papers

Enzymatic coupling of α,α-dialkyl amino acids using inverse substrates as acyl donors

Sekizaki, Haruo,Itoh, Kunihiko,Toyota, Eiko,Tanizawa, Kazutaka

, p. 1777 - 1780 (2007/10/03)

Two series of inverse substrates, N(α)-Boc-α,α-dialkyl amino acid p-guanidino- and p-(guanidinomethyl)phenyl esters, were prepared as acyl donor components for enzymatic peptide synthesis. They were found to be readily coupled with amino acid p-nitroanili

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