Cas 1262996-46-2,(S)-5-(4-(6-(2-tert-butoxycarbonylamino-3-phenylpropanoyloxy)hexyloxy)phenyl)-[2,2':5',2'']-terthiophene

1262996-46-2

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Basic information

Product Name: (S)-5-(4-(6-(2-tert-butoxycarbonylamino-3-phenylpropanoyloxy)hexyloxy)phenyl)-[2,2':5',2'']-terthiophene
Synonyms: (S)-5-(4-(6-(2-tert-butoxycarbonylamino-3-phenylpropanoyloxy)hexyloxy)phenyl)-[2,2':5',2'']-terthiophene
CAS NO:1262996-46-2
Molecular Formula:
Molecular Weight: 687.945
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: (S)-5-(4-(6-(2-tert-butoxycarbonylamino-3-phenylpropanoyloxy)hexyloxy)phenyl)-[2,2':5',2'']-terthiophene(CAS DataBase Reference)
NIST Chemistry Reference: (S)-5-(4-(6-(2-tert-butoxycarbonylamino-3-phenylpropanoyloxy)hexyloxy)phenyl)-[2,2':5',2'']-terthiophene(1262996-46-2)
EPA Substance Registry System: (S)-5-(4-(6-(2-tert-butoxycarbonylamino-3-phenylpropanoyloxy)hexyloxy)phenyl)-[2,2':5',2'']-terthiophene(1262996-46-2)

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: 1262996-46-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262996-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,9,9 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1262996-46:
(9*1)+(8*2)+(7*6)+(6*2)+(5*9)+(4*9)+(3*6)+(2*4)+(1*6)=192
192 % 10 = 2
So 1262996-46-2 is a valid CAS Registry Number.

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1262996-46-2Relevant academic research and scientific papers

Synthesis of d-glucose and l-phenylalanine substituted phenylene-thiophene oligomers

Hassan Omar, Omar,Babudri, Francesco,Farinola, Gianluca M.,Naso, Francesco,Operamolla, Alessandra,Pedone, Adriana

, p. 486 - 494 (2011/03/18)

Phenylene-thiophene oligomers bearing peracetylated β-d-glucose or N-BOC-l-phenylalanine as chiral substituents were synthesized in good yields by a versatile protocol based on the Suzuki-Miyaura cross-coupling reaction. Aryl iodides bearing the chiral bi

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