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10405-85-3

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10405-85-3 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 108, p. 1322, 1986 DOI: 10.1021/ja00266a047Synthesis, p. 1025, 1982 DOI: 10.1055/s-1982-30049

Check Digit Verification of cas no

The CAS Registry Mumber 10405-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,0 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10405-85:
(7*1)+(6*0)+(5*4)+(4*0)+(3*5)+(2*8)+(1*5)=63
63 % 10 = 3
So 10405-85-3 is a valid CAS Registry Number.
InChI:InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h7,9H,3-6,8H2,1-2H3/b9-7-

10405-85-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name TRANS-4-NONENE

1.2 Other means of identification

Product number -
Other names 4-Nonene, (E)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10405-85-3 SDS

10405-85-3Relevant articles and documents

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Seyfert,D.,Prokai,B.

, p. 1834 - 1835 (1966)

-

Reduction of Alkynes by a New Reducing System: Calcium Metal in Amines

Benkeser, Robert A.,Belmonte, Frank G.

, p. 1662 - 1664 (1984)

-

Katz et al.

, p. 2817 (1974)

VACUUM FLASH PYROLYSIS (VFP) OF MALONYL PEROXIDES: DECARBOXYLATION VERSUS DECARBONYLATION OF THE INTERMEDIARY α-LACTONES

Adam, Waldemar,Cadiz, Carlos,Mazenod, Francois

, p. 1203 - 1206 (1981)

Vacuum Flash Pyrolysis (VFP) at ca. 450-500 deg C and ca. 0.1-0.3 Torr of spirocyclic malonyl peroxides (2a,b) affords high yields of allenes (5a,b), while the simple malonyl peroxide (2c) leads to ketone (4), derived respectively from decarboxylation of the intermediary α-lactones (3).

Debromination of vic-Dibromides with Zinc and a Catalytic Amount of Titanium(IV) Chloride in Tetrahydrofuran

Sato, Fumie,Akiyama, Toshio,Iida, Katsumi,Sato, Masao

, p. 1025 - 1026 (1982)

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Boosting the Metathesis Activity of Molybdenum Oxo Alkylidenes by Tuning the Anionic Ligand σ Donation

De Jesus Silva, Jordan,Pucino, Margherita,Zhai, Feng,Mance, Deni,Berkson, Zachariah J.,Nater, Darryl F.,Hoveyda, Amir H.,Copéret, Christophe,Schrock, Richard R.

, p. 6875 - 6880 (2021)

The catalytic performances of molecular and silica-supported molybdenum oxo alkylidene species bearing anionic O ligands [ORF9, OTPP, OHMT - where ORF9 = OC(CF3)3, OTPP = 2,3,5,6-tetraphenylphenoxy, OHMT = hexamethylterphenoxy] with different σ-donation a

Radical Addition of N-Chlorophthalimide and N-Bromophthalimide to Alkenes

Kirsch, Andre,Luening, Ulrich

, p. 129 - 134 (2007/10/03)

The addition of N-chlorophthalimide (1b) to alkenes 3 via phthalimidyl radicals introduces a chlorine atom and an imidyl moiety to vicinal C-atoms of a carbon chain. The yields depend on the substituents of the alkene 3. The regioselectivity can be explained by steric and electronic effects; differences in the behavior of the addition of N-chlorophthalimide (1b) and N-bromophthalimide (1a) can be explained by a reversible attack of the phthalimidyl radical to the double bond.

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