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49678-04-8

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49678-04-8 Usage

Chemical Properties

Light Yellow Solid

Check Digit Verification of cas no

The CAS Registry Mumber 49678-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,7 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49678-04:
(7*4)+(6*9)+(5*6)+(4*7)+(3*8)+(2*0)+(1*4)=168
168 % 10 = 8
So 49678-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrO/c10-9-5-3-8(4-6-9)2-1-7-11/h1-7H/b2-1+

49678-04-8 Well-known Company Product Price

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  • TCI America

  • (B4337)  trans-4-Bromocinnamaldehyde  >98.0%(GC)

  • 49678-04-8

  • 1g

  • 350.00CNY

  • Detail
  • TCI America

  • (B4337)  trans-4-Bromocinnamaldehyde  >98.0%(GC)

  • 49678-04-8

  • 5g

  • 1,100.00CNY

  • Detail

49678-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-4-Bromocinnamaldehyde

1.2 Other means of identification

Product number -
Other names 3-(4-bromophenyl)acrylaldehyde

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:49678-04-8 SDS

49678-04-8Relevant articles and documents

Synthesis and biological evaluation of novel radioiodinated benzimidazole derivatives for imaging α-synuclein aggregates

Watanabe, Hiroyuki,Ariyoshi, Taisuke,Ozaki, Akihiko,Ihara, Masafumi,Ono, Masahiro,Saji, Hideo

, p. 6398 - 6403 (2017)

α-Synuclein (α-syn) aggregates are commonly found in the brains of patients with Parkinson's disease (PD), dementia with Lewy bodies (DLB), and some other diseases. Therefore, in vivo imaging of α-syn aggregates would aid in drug development, early diagno

Cis-Enals in N-heterocyclic carbene-catalyzed reactions: Distinct stereoselectivity and reactivity

Chen, Xingkuan,Fang, Xinqiang,Chi, Yonggui Robin

, p. 2613 - 2618 (2013)

The first successful generation of cis-homoenolate equivalents from cis-enals under the catalysis of N-heterocyclic carbenes (NHCs) has been realized. The cis-homoenolate intermediates undergo effective reactions with α,β-unsaturated imines to afford chir

Substrate-Controlled Chemo-/Enantioselective Synthesis of α-Benzylated Enals and Chiral Cyclopropane-Fused 2-Chromanone Derivatives

Byeon, Huimyoung,Ryu, Sunghyeon,Yoo, Eun Jeong,Yang, Jung Woon

supporting information, p. 5085 - 5091 (2021/09/20)

Substrate-controlled cascade reactions between α,β-unsaturated aldehydes or their analogues and 2,4-dinitrobenzyl chloride in the presence of a chiral secondary amine as the catalyst and base were developed, to obtain a broad spectrum of α-benzylated enals and enantioenriched cyclopropane-fused chroman-2-one derivatives. The cyclopropane-tethered iminium ion clearly served as a key intermediate in these reactions to trigger stereochemical outcomes, one of which was supported by a control experiment. (Figure presented.).

Asymmetric Synthesis of Functionalized 9-Methyldecalins Using a Diphenylprolinol-Silyl-Ether-Mediated Domino Michael/Aldol Reaction

Hayashi, Yujiro,Salazar, Hugo A.,Koshino, Seitaro

supporting information, p. 6654 - 6658 (2021/09/11)

Substituted 9-methyldecalin derivatives containing an all carbon quaternary chiral center were synthesized with excellent enantioselectivity via an organocatalyst-mediated domino reaction. The first reaction is a diphenylprolinol silyl ether-mediated Michael reaction, and the second reaction is an intramolecular aldol reaction. The enantiomerically pure catalyst is involved in both reactions.

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