Cas 78311-46-3,(Z)-2-(8-Methyl-1,3-diphenyl-8λ<sup>4</sup>-thia-dibenzo[e,h]azulen-2-yl)-but-2-enedioic acid dimethyl ester

78311-46-3

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Basic information

Product Name: (Z)-2-(8-Methyl-1,3-diphenyl-8λ⁴-thia-dibenzo[e,h]azulen-2-yl)-but-2-enedioic acid dimethyl ester
Synonyms:
CAS NO:78311-46-3
Molecular Formula:
Molecular Weight: 556.682
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: (Z)-2-(8-Methyl-1,3-diphenyl-8λ⁴-thia-dibenzo[e,h]azulen-2-yl)-but-2-enedioic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(8-Methyl-1,3-diphenyl-8λ⁴-thia-dibenzo[e,h]azulen-2-yl)-but-2-enedioic acid dimethyl ester(78311-46-3)
EPA Substance Registry System: (Z)-2-(8-Methyl-1,3-diphenyl-8λ⁴-thia-dibenzo[e,h]azulen-2-yl)-but-2-enedioic acid dimethyl ester(78311-46-3)

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: 78311-46-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78311-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,1 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78311-46:
(7*7)+(6*8)+(5*3)+(4*1)+(3*1)+(2*4)+(1*6)=133
133 % 10 = 3
So 78311-46-3 is a valid CAS Registry Number.

78311-46-3Upstream product

78311-46-3Downstream Products

78311-48-5 (Z)-2-(3a-Methyl-1,3-diphenyl-3aH-8-thia-dibenzo[e,h]azulen-2-yl)-but-2-enedioic acid dimethyl ester

78311-46-3Relevant academic research and scientific papers

REACTION OF NEW CYCLIC SULFUR YLIDES, 8-THIAAZULENES WITH ELECTROPHILES

Hori, Mikio,Kataoka, Tadashi,Shimizu, Hiroshi,Okitsu, Mitsuhito

, p. 721 - 724 (2007/10/02)

The reactions of 8-alkyl-1,3-diphenyldibenzo-8-thiaazulenes with acetylenic electrophiles yielded the considerably stable ylides.The ylides newly formed were not rearranged on refluxing in THF for 1 h, but caused the intramolecular 1,4-rearrangement

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