Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1,7,7-Trimethyl-2-phenylbicyclo[2.2.1]hept-2-ene is a complex organic compound with the molecular formula C16H20. It is a bicyclic aromatic hydrocarbon, characterized by its unique structure consisting of two carbon rings, one of which is a six-membered ring and the other a three-membered ring. The compound features three methyl groups (CH3) attached to the carbon atoms at positions 1, 7, and 7, and a phenyl group (C6H5) attached to the carbon atom at position 2. This chemical is known for its stability and is often used in the synthesis of various pharmaceuticals and other organic compounds due to its versatile structure. It is an important intermediate in organic chemistry, particularly in the preparation of complex molecules that require a bicyclo[2.2.1]heptane framework.

7070-09-9

Post Buying Request

7070-09-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7070-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7070-09-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7070-09:
(6*7)+(5*0)+(4*7)+(3*0)+(2*0)+(1*9)=79
79 % 10 = 9
So 7070-09-9 is a valid CAS Registry Number.

7070-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7,7-trimethyl-3-phenylbicyclo[2.2.1]hept-2-ene

1.2 Other means of identification

Product number -
Other names 1,7,7-Trimethyl-2-phenylbicyclo[2.2.1]hept-2-ene

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:7070-09-9 SDS

7070-09-9Relevant articles and documents

Conversion of Carbonyl Compounds to Olefins via Enolate Intermediate

Cao, Zhi-Chao,Xu, Pei-Lin,Luo, Qin-Yu,Li, Xiao-Lei,Yu, Da-Gang,Fang, Huayi,Shi, Zhang-Jie

supporting information, p. 781 - 785 (2019/06/24)

A general and efficient protocol to synthesize substituted olefins from carbonyl compounds via nickel catalyzed C—O activation of enolates was developed. Besides ketones, aldehydes were also suitable substrates for the presented catalytic system to produce di- or tri- substituted olefins. It is worth noting that this approach exhibited good tolerance to highly reactive tertiary alcohols, which could not survive in other reported routes for converting carbonyl compounds to olefins. This method also showed good regio- and stereo-selectivity for olefin products. Preliminary mechanistic studies indicated that the reaction was accomplished through nickel catalyzed C—O activation of enolates, thus offering helpful contribution to current enol chemistry.

Enantioselective hydrogenation with chiral frustrated Lewis Pairs

Chen, Dianjun,Wang, Yutian,Klankermayer, Juergen

supporting information; experimental part, p. 9475 - 9478 (2011/02/23)

No subsequent frustration: Frustrated Lewis pairs (FLPs) have been recently introduced as an unprecedented possibility to activate hydrogen. On the basis of this concept the first example of highly enantioselective catalytic hydrogenation of imines using

Renewable camphor-derived hydroperoxide: Synthesis and use in the asymmetric epoxidation of allylic alcohols

Lattanzi, Alessandra,Iannece, Patrizia,Vicinanza, Assunta,Scettri, Arrigo

, p. 1440 - 1441 (2007/10/03)

Renewable enantiopure tertiary furyl hydroperoxide has been easily synthesized in two steps starting from low cost (+)-(1R)-camphor and it has been used in the asymmetric epoxidation and kinetic resolution of allylic alcohols (enantioselectivities up to 46%).

Palladium complex-catalyzed cross-coupling reaction of organobismuth dialkoxides with triflates

Rao, Maddali L. N.,Shimada, Shigeru,Tanaka, Masato

, p. 1271 - 1273 (2008/02/09)

(matrix presented) Pd(PPh3)4 catalyzes cross-coupling reaction between organobismuth alkoxides and aryl and vinyl triflates.

THE OCTANT RULE XXIII. ANTIOCTANT EFFECTS IN γ,δ-UNSATURATED KETONES

Toan, Vien Van,Lightner, David A.

, p. 5769 - 5774 (2007/10/02)

The exo and endo α-benzyl derivatives (1 and 2. respectively) of (+)-camphor have been synthesized and are found to exert a strong influence on the circular dichroism n?* Cotton effects: 1: Δε301max -0.36 (n-heptane) and 2: Δε302max +3.22, relative to camphor: Δε304max + 1.8 (n-heptane).Evidence for electric dipole transition moment coupling in these γ,δ-unsaturated systems is found in the n?* UV: 1: ε291max 84 (n-heptane) and 2: ε285max 303, relative to camphor: ε290max 25.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 7070-09-9