114095-73-7

• 

• Basic information

  1. Product Name: 4-(3-BROMOPHENYL)-1-BUTEN-4-OL
  2. Synonyms: 4-(3-BROMOPHENYL)-1-BUTEN-4-OL
  3. CAS NO:114095-73-7
  4. Molecular Formula: C₁₀H₁₁BrO
  5. Molecular Weight: 227.1
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 114095-73-7.mol
  9. Article Data: 27

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 93°C 0,1mm
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 4-(3-BROMOPHENYL)-1-BUTEN-4-OL(CAS DataBase Reference)
  10. NIST Chemistry Reference: 4-(3-BROMOPHENYL)-1-BUTEN-4-OL(114095-73-7)
  11. EPA Substance Registry System: 4-(3-BROMOPHENYL)-1-BUTEN-4-OL(114095-73-7)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: 36/37/38
  3. Safety Statements: 26-36/37/39
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 114095-73-7(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

114095-73-7 Suppliers

Recommended suppliersmore

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

114095-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114095-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,9 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114095-73:
(8*1)+(7*1)+(6*4)+(5*0)+(4*9)+(3*5)+(2*7)+(1*3)=107
107 % 10 = 7
So 114095-73-7 is a valid CAS Registry Number.

114095-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-(3-bromophenyl)-3-buten-1-ol

1.2 Other means of identification

Product number	-
Other names	1-(3-bromophenyl)but-3-en-1-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:114095-73-7 SDS

114095-73-7Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 627-15-6 1,3-dibromopropene 
• 107-05-1 3-chloroprop-1-ene 
• 762-72-1 allyl-trimethyl-silane 
• 24850-33-7 allyltributylstanane 
• 1730-25-2 allylmagnesium bromide 
• 106-95-6 allyl bromide 

114095-73-7Downstream Products

• 1251033-94-9 C₁₀H₉BrO 
• 1574316-81-6 1-(3-bromophenyl)but-3-en-1-one oxime 
• 71104-82-0 4-acetoxy-4-(m-cyanophenyl)-1-butene 
• 71104-86-4 4-methoxy-4-(m-cyanophenyl)-1-butene 
• 207994-95-4 1-(3-bromophenyl)-1-butanone 
• 114095-77-1 4-(m-bromophenyl)-4-methoxy-1-butene 
• 1262038-99-2 (1-(3-bromophenyl)but-3-enyloxy)(tert-butyl)dimethylsilane 
• 114095-74-8 3-(1-hydroxybut-3-en-1-yl)benzonitrile 

114095-73-7Relevant articles and documents

Carbon-carbon bond formation reaction promoted by cadmium in aqueous media

Zheng,Bao,Zhang

, p. 3517 - 3521 (2000)

Promoted by metallic cadmium allylilic and propargyl bromides react smoothly with aldehydes in aqueous DMF to give homoallylic and homopropargyl alcohols in moderate to good yields. It can also promote pinacol coupling of aromatic aldehydes. The metallic cadmium is produced in situ by the reduction of CdCl2 · H2O with samarium metal.

A convenient procedure for bismuth-mediated Barbier-type allylation of aldehydes in water containing fluoride ions

Smith, Keith,Lock, Sandra,El-Hiti, Gamal A.,Wada, Makoto,Miyoshi, Norikazu

, p. 935 - 938 (2004)

A new and convenient procedure for synthesis of homoallylic alcohols in generally good to excellent yields has been developed. The bismuth-mediated Barbier-type allylation of aldehydes (aromatic, aliphatic, alicyclic and heterocyclic) with allyl bromide h

Palladium-catalyzed anti-Markovnikov oxidative acetalization of activated olefins with iron(iii) sulphate as the reoxidant

Fernandes, Rodney A.,Kumar, Praveen,Yadav, Sandhya S.

, p. 427 - 443 (2022/01/20)

This paper discloses the efficient palladium-catalyzed anti-Markovnikov oxidative acetalization of activated terminal olefins with iron(iii) sulfate as the reoxidant. This methodology requires mild reaction conditions and shows high regioselectivity toward anti-Markovnikov products and compatibility with a wide range of functional groups. Iron(iii) sulphate was the sole reoxidant used in this method. Various olefins like vinylarenes, aryl-allylethers, aryl or benzyl acrylates and homoallylic alcohols all reacted well providing anti-Markovnikov acetals, some of which represent orthogonally functionalized 1,3- and 1,4-dioxygenated compounds.

Cationic Cobalt Porphyrin-Catalyzed Allylation of Aldehydes with Allyltrimethylsilanes

Tomifuji, Rei,Masuda, Shota,Kurahashi, Takuya,Matsubara, Seijiro

supporting information, p. 3834 - 3837 (2019/05/24)

Cationic cobalt porphyrin-catalyzed allylation of aldehydes with allyltrimethylsilanes is developed. The formation of the aldehyde-cobalt porphyrin complex, the key intermediate for the addition of allylsilanes, is confirmed by theoretical studies and syn

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
• Urgent purchase

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)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 114095-73-7 4-(3-BROMOPHENYL)-1-BUTEN-4-OL

Send

Send

Metric Ton KG G Pound L ML

Send

Send