Cas 915184-69-9,methyl 5-[5-(2,4-dimethoxy-benzylamino)-2,4-diisobutoxy-benzoylamino]-2,4-dimethoxybenzoate

915184-69-9

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Basic information

Product Name: methyl 5-[5-(2,4-dimethoxy-benzylamino)-2,4-diisobutoxy-benzoylamino]-2,4-dimethoxybenzoate
Synonyms: methyl 5-[5-(2,4-dimethoxy-benzylamino)-2,4-diisobutoxy-benzoylamino]-2,4-dimethoxybenzoate
CAS NO:915184-69-9
Molecular Formula:
Molecular Weight: 624.731
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: methyl 5-[5-(2,4-dimethoxy-benzylamino)-2,4-diisobutoxy-benzoylamino]-2,4-dimethoxybenzoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-[5-(2,4-dimethoxy-benzylamino)-2,4-diisobutoxy-benzoylamino]-2,4-dimethoxybenzoate(915184-69-9)
EPA Substance Registry System: methyl 5-[5-(2,4-dimethoxy-benzylamino)-2,4-diisobutoxy-benzoylamino]-2,4-dimethoxybenzoate(915184-69-9)

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: 915184-69-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915184-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,1,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 915184-69:
(8*9)+(7*1)+(6*5)+(5*1)+(4*8)+(3*4)+(2*6)+(1*9)=179
179 % 10 = 9
So 915184-69-9 is a valid CAS Registry Number.

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915184-69-9Relevant academic research and scientific papers

Improving foldamer synthesis through protecting group induced unfolding of aromatic oligoamides

Zhang, Aimin,Ferguson, Joseph S.,Yamato, Kazuhiro,Zheng, Chong,Gong, Bing

, p. 5117 - 5120 (2007/10/03)

(Chemical Equation Presented) The hydrogen bond rigidified backbones of aromatic oligoamides are temporarily interrupted by replacing the amide hydrogens with the acid-labile 2,4-dimethoxybenzyl (DMB) group, which allows the efficient preparation of long

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