Cas 191277-08-4,4-({(4-tert-Butoxycarbonylamino-butyl)-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-benzoic acid methyl ester

191277-08-4

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Basic information

Product Name: 4-({(4-tert-Butoxycarbonylamino-butyl)-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-benzoic acid methyl ester
Synonyms: 4-({(4-tert-Butoxycarbonylamino-butyl)-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-benzoic acid methyl ester
CAS NO:191277-08-4
Molecular Formula:
Molecular Weight: 567.639
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: 4-({(4-tert-Butoxycarbonylamino-butyl)-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-benzoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-({(4-tert-Butoxycarbonylamino-butyl)-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-benzoic acid methyl ester(191277-08-4)
EPA Substance Registry System: 4-({(4-tert-Butoxycarbonylamino-butyl)-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-benzoic acid methyl ester(191277-08-4)

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: 191277-08-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 191277-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,2,7 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 191277-08:
(8*1)+(7*9)+(6*1)+(5*2)+(4*7)+(3*7)+(2*0)+(1*8)=144
144 % 10 = 4
So 191277-08-4 is a valid CAS Registry Number.

191277-08-4Upstream product

191277-08-4Downstream Products

201211-60-1 N¹-phthalamic acid-N⁴-(4-benzyloxycarbonyl-1-benzoic acid)-N⁸-Boc-spermidine

191277-08-4Relevant academic research and scientific papers

Solid phase synthesis of polyamine conjugates for the study of trypanothione reductase

Marsh, Ian R.,Bradley, Mark

, p. 17317 - 17334 (2007/10/03)

A number of polyamine scaffolds were synthesised, enabling the facile preparation of a variety of polyamine conjugates using both Boc and Fmoc protecting group strategies. Products were released from the solid support by treatment with either triflic acid/trifluoroacetic acid or trifluoroacetic acid. The trypanosomal metabolite N1, N6-bis(glurathionyl)spermidine [trypanothione], and a range of related analogues were prepared for biological evaluation as previously communicated.

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