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Benzenemethanol, a-[bis(phenylthio)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13307-64-7

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13307-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13307-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13307-64:
(7*1)+(6*3)+(5*3)+(4*0)+(3*7)+(2*6)+(1*4)=77
77 % 10 = 7
So 13307-64-7 is a valid CAS Registry Number.

13307-64-7SDS

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 1-phenyl-2,2-bis(phenylthio)ethanol

1.2 Other means of identification

Product number -
Other names α-Phenyl-α-hydroxy-acetaldehyd-diphenylthioacetal

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:13307-64-7 SDS

13307-64-7Relevant academic research and scientific papers

Copper-Catalyzed Synthesis of gem-Bisarylthio Enamines under Redox-Neutral Conditions

Ni, Jiabin,Mao, Xiaokang,Zhang, Ao

supporting information, p. 2004 - 2008 (2019/03/21)

An efficient approach for the construction of gem-bisarylthio enamines via coupling of oxime acetates with diaryl disulfides is developed. This process involved copper-catalyzed N?O/S?S bond cleavages and formation of two new C?S bonds. A broad range of s

Nucleophilic fluoromethylation of aldehydes with fluorobis(phenylsulfonyl) methane: The importance of strong Li-O coordination and fluorine substitution for C-C bond formation

Shen, Xiao,Zhang, Laijun,Zhao, Yanchuan,Zhu, Lingui,Li, Guangyu,Hu, Jinbo

supporting information; experimental part, p. 2588 - 2592 (2011/04/25)

The tighter, the better! Fluorobis(phenylsulfonyl)methane reacts readily with aldehydes to give addition products in excellent yields (see scheme; LiHMDS=lithium hexamethyldisilazide), which is in sharp contrast to previous findings. Both strong Li-O coordination at low temperature and fluorine substitution play important roles in successful C-C bond formation. Copyright

Mechanistic Insight into Allylmetal-Thioacetal Reactions Employing 2-Acetoxy-2-phenylacetaldehyde Thioacetals

Sato, Tsuneo,Otera, Junzo,Nozaki, Hitosi

, p. 6116 - 6121 (2007/10/02)

The mechanism of allyl-metal-thioacetal reactions has been investigated by using 2-acetoxy-2-phenylacetaldehyde thioacetals in the presence of trimethylsilyl triflate.The results unambiguously revealed the occurence of both SN1- and SN/su

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