Cas 124615-87-8,Formic acid 3-[{4-[(3-formyloxy-propyl)-(toluene-4-sulfonyl)-amino]-butyl}-(toluene-4-sulfonyl)-amino]-propyl ester

124615-87-8

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Basic information

Product Name: Formic acid 3-[{4-[(3-formyloxy-propyl)-(toluene-4-sulfonyl)-amino]-butyl}-(toluene-4-sulfonyl)-amino]-propyl ester
Synonyms: Formic acid 3-[{4-[(3-formyloxy-propyl)-(toluene-4-sulfonyl)-amino]-butyl}-(toluene-4-sulfonyl)-amino]-propyl ester
CAS NO:124615-87-8
Molecular Formula:
Molecular Weight: 568.712
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: Formic acid 3-[{4-[(3-formyloxy-propyl)-(toluene-4-sulfonyl)-amino]-butyl}-(toluene-4-sulfonyl)-amino]-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Formic acid 3-[{4-[(3-formyloxy-propyl)-(toluene-4-sulfonyl)-amino]-butyl}-(toluene-4-sulfonyl)-amino]-propyl ester(124615-87-8)
EPA Substance Registry System: Formic acid 3-[{4-[(3-formyloxy-propyl)-(toluene-4-sulfonyl)-amino]-butyl}-(toluene-4-sulfonyl)-amino]-propyl ester(124615-87-8)

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: 124615-87-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124615-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124615-87:
(8*1)+(7*2)+(6*4)+(5*6)+(4*1)+(3*5)+(2*8)+(1*7)=118
118 % 10 = 8
So 124615-87-8 is a valid CAS Registry Number.

124615-87-8Upstream product

107976-56-7 N,N'-bis(3-formamidopropyl)-N,N'-ditosyl-1,4-butanediamine

124615-87-8Downstream Products

84395-88-0 N⁴,N⁹-ditosyl-4,9-diaza-1,12-dodecanediol

124615-87-8Relevant academic research and scientific papers

Conversion of Formamides to Alcohols via N-Nitrosation

Iwata, Masaaki,Kuzuhara, Hiroyoshi

, p. 1195 - 1198 (2007/10/02)

Secondary formamides were found to be favorable sources for the efficient oxygenation site via N-nitrosation.Thermal reaction (85 deg C in benzene) of N-nitrozo formamides proceeded effectively to provide the corresponding formates in good yields, which, then, were hydrolyzed to alcohols under weakly basic conditions.In treatment of optically active formamide, the corresponding alcohol was isolated with 72percent retention of configuration.

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