Cas 1439902-75-6,(2S,2’S)-2,2’-(4,4’-((isophthaloylbis(azanediyl))bis(methylene))bis(1H-1,2,3-triazole-4,1-diyl))bis(3-(4-hydroxyphenyl)propanoicacid)

1439902-75-6

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Basic information

Product Name: (2S,2’S)-2,2’-(4,4’-((isophthaloylbis(azanediyl))bis(methylene))bis(1H-1,2,3-triazole-4,1-diyl))bis(3-(4-hydroxyphenyl)propanoicacid)
Synonyms:
CAS NO:1439902-75-6
Molecular Formula:
Molecular Weight: 654.639
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: (2S,2’S)-2,2’-(4,4’-((isophthaloylbis(azanediyl))bis(methylene))bis(1H-1,2,3-triazole-4,1-diyl))bis(3-(4-hydroxyphenyl)propanoicacid)(CAS DataBase Reference)
NIST Chemistry Reference: (2S,2’S)-2,2’-(4,4’-((isophthaloylbis(azanediyl))bis(methylene))bis(1H-1,2,3-triazole-4,1-diyl))bis(3-(4-hydroxyphenyl)propanoicacid)(1439902-75-6)
EPA Substance Registry System: (2S,2’S)-2,2’-(4,4’-((isophthaloylbis(azanediyl))bis(methylene))bis(1H-1,2,3-triazole-4,1-diyl))bis(3-(4-hydroxyphenyl)propanoicacid)(1439902-75-6)

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: 1439902-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1439902-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,9,9,0 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1439902-75:
(9*1)+(8*4)+(7*3)+(6*9)+(5*9)+(4*0)+(3*2)+(2*7)+(1*5)=186
186 % 10 = 6
So 1439902-75-6 is a valid CAS Registry Number.

1439902-75-6Upstream product

1439902-73-4 (2S,2’S)-2,2’-(4,4’-((isophthaloylbis(azanediyl))bis(methylene))bis(1H-1,2,3-triazole-4,1-diyl))bis(3-(4-hydroxyphenyl)propanoate)methyl diester

1439902-75-6Downstream Products

1439902-75-6Relevant academic research and scientific papers

Click synthesis of triazolyl phenylalaninyl and tyrosinyl derivatives as new protein tyrosine phosphatase inhibitors

Cui, Lei,He, Xiao-Peng,Gao, Li-Xin,Li, Jia,Chen, Guo-Rong

, p. 684 - 688 (2013)

The efficient construction of triazolyl peptidomimetics via the powerful click chemistry for the discovery of small molecule-based chemotherapeutic agents represents a promising strategy in drug development today. Herein, the synthesis of novel mono-triaz

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