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816419-99-5

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816419-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 816419-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,6,4,1 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 816419-99:
(8*8)+(7*1)+(6*6)+(5*4)+(4*1)+(3*9)+(2*9)+(1*9)=185
185 % 10 = 5
So 816419-99-5 is a valid CAS Registry Number.

816419-99-5SDS

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 tris(hept-6-enyl)phosphane

1.2 Other means of identification

Product number -
Other names Phosphine,tri-6-heptenyl

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:816419-99-5 SDS

816419-99-5Relevant articles and documents

Molecular gyroscopes: {Fe(CO)3} and {Fe(CO)2(NO)} + rotators encased in three-spoke stators; facile assembly by alkene metatheses

Shima, Takanori,Hampel, Frank,Gladysz

, p. 5537 - 5540 (2004)

Complexes to toy with: Ring-closing metathesis of the bis(phosphane) complexes 1a-c (n = 4-6) followed by hydrogenation gives the "molecular gyroscopes" 2a-c. The crystal structure of 2c and the NMR data for the analogous {Fe(CO)2(NO)}+/s

Syntheses and palladium, platinum, and borane adducts of symmetrical trialkylphosphines with three terminal vinyl groups, P((CH2) mCH=CH2)3

Nawara-Hultzsch, Agnieszka J.,Skopek, Katrin,Shima, Takanori,Barbasiewicz, Micha,Hess, Gisela D.,Skaper, Dirk,Gladysz, John A.

experimental part, p. 414 - 424 (2010/10/01)

Reactions of Br(CH2)mCH=CH2 with Mg powder and then PCl3 (0.33 equiv.) afford P((CH2)m-CH=CH 2)3 (1; m = a, 4; b, 5; c, 6; d, 7; e, 8; f, 9; 52-87 %). Reactions of 1a-c, e with PdX2(COD) (X = Cl, Br) give trans-PdX 2(P((CH2)mCH=CH2)3) 2 (35-92 %). Reactions of 1b-e with PtCl2 in benzene give mainly trans-PtCl2(P((CH2)mCH=CH 2)3)2 (trans-5b-e; 52-75 %), whereas those with K2PtCl4 in water give mainly cis-5b-e (33-70 %). The reaction of equimolar quantities of 1c and H3B.S(CH3) 2 gives the 1 : 1 adduct H3B·P((CH 2)6CH=CH2)3 (85 %). In none of these transformations are by-products derived from the C=C linkages observed.

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