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1-Penten-3-ol, 5-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117661-29-7

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117661-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117661-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,6 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 117661-29:
(8*1)+(7*1)+(6*7)+(5*6)+(4*6)+(3*1)+(2*2)+(1*9)=127
127 % 10 = 7
So 117661-29-7 is a valid CAS Registry Number.

117661-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylmethoxypent-1-en-3-ol

1.2 Other means of identification

Product number -
Other names 1-benzyloxy-4-penten-3-ol

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:117661-29-7 SDS

117661-29-7Relevant academic research and scientific papers

A highly stereoselective synthesis of Z-disubstituted olefin by O-assisted Still-Wittig rearrangement

Fujii, Kazushige,Hara, Osamu,Fujita, Yoko,Sakagami, Youji

, p. 389 - 392 (1996)

In the Still-Wittig rearrangement, stannylated methyl (E)-allylic ethers having an aliphatic side chain (1a-c) exhibited the usual similar stereoselectivity, although the poor stereoselectivity was remarkably improved by the assistance of an alkoxy moiety on the alkenyl chain. A stannylated methyl (Z)-allylic ether bearing an alkoxy moiety on the alkenyl chain (1e) also showed a high E selectivity as previously reported.

Regio- And Enantioselective Iridium-Catalyzed Amination of Alkyl-Substituted Allylic Acetates with Secondary Amines

Jung, Woo-Ok,Yoo, Minjin,Migliozzi, Madyson M.,Zbieg, Jason R.,Stivala, Craig E.,Krische, Michael J.

supporting information, p. 441 - 445 (2021/12/27)

Robust air-stable cyclometalated π-allyliridium C,O-benzoates modified by (S)-tol-BINAP catalyze the reaction of secondary aliphatic amines with racemic alkyl-substituted allylic acetates to furnish products of allylic amination with high levels of enantioselectivity. Complete branched regioselectivities were observed despite the formation of more highly substituted C-N bonds.

Visible-Light Photoredox-Catalyzed α-Regioselective Conjugate Addition of Allyl Groups to Activated Alkenes

Gontala, Arjun,Woo, Sang Kook

supporting information, p. 3223 - 3228 (2020/07/06)

The α-regioselective conjugate addition of allyl groups to activated alkenes is a poorly explored area of research. Herein, we report an α-adduct and (E)-isomer selective conjugate addition of allylsilanes to activated alkenes by visible-light photoredox catalysis. The reaction involves allylic radicals that can be generated from allylsilanes through a photoinduced single-electron transfer mechanism. (Figure presented.).

Catalytic Hydroetherification of Unactivated Alkenes Enabled by Proton-Coupled Electron Transfer

Knowles, Robert R.,Metrano, Anthony J.,Tsuchiya, Yuto,Tsui, Elaine

supporting information, p. 11845 - 11849 (2020/05/22)

We report a catalytic, light-driven method for the intramolecular hydroetherification of unactivated alkenols to furnish cyclic ether products. These reactions occur under visible-light irradiation in the presence of an IrIII-based photoredox catalyst, a Br?nsted base catalyst, and a hydrogen-atom transfer (HAT) co-catalyst. Reactive alkoxy radicals are proposed as key intermediates, generated by direct homolytic activation of alcohol O?H bonds through a proton-coupled electron-transfer mechanism. This method exhibits a broad substrate scope and high functional-group tolerance, and it accommodates a diverse range of alkene substitution patterns. Results demonstrating the extension of this catalytic system to carboetherification reactions are also presented.

C-20 STEROID COMPOUNDS, COMPOSITIONS AND USES THEREOF TO TREAT TRAUMATIC BRAIN INJURY (TBI), INCLUDING CONCUSSIONS

-

, (2016/04/09)

The present invention relates to C-20 steroid compounds, compositions and methods of use thereof to treat, minimize and/or prevent traumatic brain injury (TBI), including severe TBI, moderate TBI and mild TBI, including concussions.

A Modular Synthesis of Some Biologically Relevant Cyclic Peptides through Late-Stage Functionalization

Mukherjee, Jyoti Prasad,Sil, Suman,Pahari, Amit K.,Chattopadhyay, Shital K.

, p. 1181 - 1190 (2016/05/11)

A modular synthesis of some cyclic peptides related to a class of histone deacetylase inhibitors is reported. The synthesis utilizes a late-stage functionalization of a cyclic tetrapeptide scaffold to link the pendant alkyl chain through cross metathesis. It is observed that while the cross-metathesis reaction of a terminal olefin having a β-substituent is marginally successful with the scaffold, the corresponding reaction with an α,β-unsaturated ketone/ester is more promising. The utility of the protocol is demonstrated through the preparation of three cyclic tetrapeptides structurally related to the novel histone deacetylase inhibitors FR-225497 and trapoxin B.

C-20 STEROID COMPOUNDS, COMPOSITIONS, AND USES THEREOF TO TREAT TRAUMATIC BRAIN INJURY (TBI), INCLUDING CONCUSSIONS

-

, (2017/01/09)

The present invention relates to C-20 steroid compounds, compositions and methods of use thereof to treat, minimize and/or prevent traumatic brain injury (TBI), including severe TBI, moderate TBI and mild TBI, including concussions.

SYNTHESIS OF ENT-PROGESTERONE AND INTERMEDIATES THEREOF

-

, (2015/07/02)

The present invention relates to the synthesis of ent-progesterone and intermediates thereof.

A stereoselective aldol approach for the total syntheses of two 6-Alkylated 2H-pyran-2-ones

Rajaram, Singanaboina,Ramesh, Dasari,Ramulu, Udugu,Prabhakar, Peddikotla,Venkateswarlu, Yenamandra

, p. 112 - 121 (2014/02/14)

A simple and highly efficient stereoselective total synthesis of the 6-alkylated pyranones (6R)-6-[(1E,4R,6R)-4,6-dihydroxy-10-phenyldec-1-en-1-yl]- 5,6-dihydro-2H-pyran-2-one (1) and (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6- phenylhexyl]-2H-pyran-2-one (2) w

A convergent and stereoselective total synthesis of phomolides G and H

Subba Reddy,Sivaramakrishna Reddy,Phaneendra Reddy,Yadav

, p. 501 - 504 (2014/03/21)

A stereoselective total synthesis of phomolides G and H, a polyketide natural products is described. The synthesis involves organocatalytic enantioselective asymmetric epoxidation, C1-Wittig olefination, and ring-closing metathesis as key steps. The use of organocatalytic MacMillan asymmetric epoxidation for the construction of two chiral centers of phomolides G and H makes this approach more attractive. Georg Thieme Verlag Stuttgart New York.

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