Cas 134918-32-4,16-(Toluene-4-sulfonyl)-2,6-dioxa-13,16,19-triaza-tricyclo[18.4.0.07,12]tetracosa-1(24),7(12),8,10,20,22-hexaen-4-ol

134918-32-4

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Basic information

Product Name: 16-(Toluene-4-sulfonyl)-2,6-dioxa-13,16,19-triaza-tricyclo[18.4.0.0^7,12]tetracosa-1⁽²⁴⁾,7⁽¹²⁾,8,10,20,22-hexaen-4-ol
Synonyms:
CAS NO:134918-32-4
Molecular Formula:
Molecular Weight: 497.615
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: 16-(Toluene-4-sulfonyl)-2,6-dioxa-13,16,19-triaza-tricyclo[18.4.0.0^7,12]tetracosa-1⁽²⁴⁾,7⁽¹²⁾,8,10,20,22-hexaen-4-ol(CAS DataBase Reference)
NIST Chemistry Reference: 16-(Toluene-4-sulfonyl)-2,6-dioxa-13,16,19-triaza-tricyclo[18.4.0.0^7,12]tetracosa-1⁽²⁴⁾,7⁽¹²⁾,8,10,20,22-hexaen-4-ol(134918-32-4)
EPA Substance Registry System: 16-(Toluene-4-sulfonyl)-2,6-dioxa-13,16,19-triaza-tricyclo[18.4.0.0^7,12]tetracosa-1⁽²⁴⁾,7⁽¹²⁾,8,10,20,22-hexaen-4-ol(134918-32-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 134918-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134918-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,1 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134918-32:
(8*1)+(7*3)+(6*4)+(5*9)+(4*1)+(3*8)+(2*3)+(1*2)=134
134 % 10 = 4
So 134918-32-4 is a valid CAS Registry Number.

134918-32-4Upstream product

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134918-32-4Relevant academic research and scientific papers

SYNTHESIS OF MACROHETEROCYCLIC ANALOGS OF DIBENZO-CROWN COMPOUNDS. 6. HYDROXYLATED 16-MEMBERED OXAAZA-CROWN COMPOUNDS

Formanovskii, A. A.,Mikhura, I. V.

, p. 227 - 231 (2007/10/02)

High-dilution cycloacylation of 2-acetoxy-1,3-bis-(2-aminophenoxy)propane with the diacid chlorides of glutaric, diglycolic, thiodiglycolic, and N-tosyliminodiacetic acids gives the macrocyclic diamides.Subsequent reduction with boron hydride affords 16-m

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