Cas 126644-88-0,Benzene, [(3-methylpentyl)sulfonyl]-

126644-88-0

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Basic information

Product Name: Benzene, [(3-methylpentyl)sulfonyl]-
Synonyms:
CAS NO:126644-88-0
Molecular Formula: C12H18O2S
Molecular Weight: 226.34
EINECS: N/A
Product Categories: N/A
Mol File: 126644-88-0.mol

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: Benzene, [(3-methylpentyl)sulfonyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzene, [(3-methylpentyl)sulfonyl]-(126644-88-0)
EPA Substance Registry System: Benzene, [(3-methylpentyl)sulfonyl]-(126644-88-0)

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: 126644-88-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126644-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,6,4 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126644-88:
(8*1)+(7*2)+(6*6)+(5*6)+(4*4)+(3*4)+(2*8)+(1*8)=140
140 % 10 = 0
So 126644-88-0 is a valid CAS Registry Number.

126644-88-0Upstream product

126644-88-0Downstream Products

126644-88-0Relevant academic research and scientific papers

Zn/CuI-mediated coupling of alkyl halides with vinyl sulfones, vinyl sulfonates, and vinyl sulfonamides

Zhao, Matthew M.,Qu, Chuanxing,Lynch, Joseph E.

, p. 6944 - 6947 (2007/10/03)

A novel high-yielding Zn/CuI-mediated coupling method of alkyl halides with vinyl sulfones, vinyl sulfonates, and vinyl sulfonamides is described. This protocol is applicable for primary, secondary, and tertiary alkyl iodides and bromides. Alkyl chlorides

Indium as a radical initiator in aqueous media: Intermolecular alkyl radical addition to C=N and C=C bond

Miyabe, Hideto,Ueda, Masafumi,Nishimura, Azusa,Naito, Takeaki

, p. 4227 - 4235 (2007/10/03)

The carbon-carbon bond-forming method in aqueous media was investigated by using indium as a single-electron transfer radical initiator. The indium-mediated intermolecular alkyl radical addition to imine derivatives and electron-deficient C=C bond proceeded effectively.

Indium-mediated intermolecular alkyl radical addition to electron-deficient C=N bond and C=C bond in water

Miyabe, Hideto,Ueda, Masafumi,Nishimura, Azusa,Naito, Takeaki

, p. 131 - 133 (2007/10/03)

(matrix presented) The intermolecular alkyl radical addition to imine derivatives was studied in aqueous media by using indium as a single-electron-transfer radical initiator. The one-pot reaction based on radical addition to glyoxylic hydrazone provided a convenient method for preparing the α-amino acids. The indium-mediated radical addition to an electron-deficient C=C bond also proceeded effectively to provide the new carbon-carbon bond-forming method in aqueous media.

Directed Lithiation of Chlorobenzenes. Regioselectivity and Application to a Short Synthesis of Benzocyclobutenes

Iwao, Masatomo

, p. 3622 - 3627 (2007/10/02)

Chlorobenzene and its OMe, OSiMe2-t-Bu, and Cl derivatives 1 were lithiated with high regioselectivity ortho to chlorine by treatment with sec-BuLi in THF at -105 deg C without complications due to benzyne formation.The lithio species thus generated under

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