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6331-99-3

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6331-99-3 Usage

Physical state

Colorless liquid

Aroma

Minty

Common uses

Flavor and fragrance ingredient in perfumes, cosmetics, and personal care products

Source

Found in natural sources such as mint oil

Chemical classification

Allyl alcohol derivative

Antimicrobial properties

Potential use as an antimicrobial agent in various applications

Check Digit Verification of cas no

The CAS Registry Mumber 6331-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6331-99:
(6*6)+(5*3)+(4*3)+(3*1)+(2*9)+(1*9)=93
93 % 10 = 3
So 6331-99-3 is a valid CAS Registry Number.

6331-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Imidazole,2-methyl-1-triphenylmethyl

1.2 Other means of identification

Product number -
Other names 2-Methyl-1-trityl-1H-imidazole

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:6331-99-3 SDS

6331-99-3Relevant articles and documents

Stereoselective Dehydroxyboration of Allylic Alcohols to Access (E)-Allylboronates by a Combination of C-OH Cleavage and Boron Transfer under Iron Catalysis

Su, Wei,Wang, Ting-Ting,Tian, Xia,Han, Jian-Rong,Zhen, Xiao-Li,Fan, Shi-Ming,You, Ya-Xin,Zhang, Yu-Kun,Qiao, Rui-Xiao,Cheng, Qiushi,Liu, Shouxin

supporting information, p. 9094 - 9099 (2021/11/30)

Iron-catalyzed direct SN2′ dehydroxyboration of allylic alcohols has been developed to access (E)-stereoselective allylboronates. Allylic alcohols with diverse structures and functional groups, especially derived from natural products, underwent smooth transformation. The six-membered ring transition state formed by allylic alcohols and iron-boron intermediate was indicated to be the key component involved in transfer of the boron group, activation of the C-OH bond, and control of the stereoselectivity.

Synthesis of spirocyclic butenolides by ring closing metathesis

Langer, Peter,Albrecht, Uwe

, p. 1841 - 1842 (2007/10/03)

Spirocyclic butenolides were efficiently prepared by a ring closing metathesis strategy.

PALLADIUM(II) CATALYZED ALLYLIC REARRANGEMENT: STEREOSELECTIVE SYNTHESIS OF 2-SUBSTITUTED (E)-β-ACETOXY (OR BENZOYLOXY)ETHYLIDENECYCLOHEXANES

Tamaru, Y.,Yamada, Y.,Ochiai, H.,Nakajo, E.,Yoshida, Z.

, p. 1791 - 1794 (2007/10/02)

Diastereoisomeric mixtures of 2-substituted 1-vinylcyclohexyl acetates (or benzoates) are rearranged stereoselectively to 2-substituted (E)-β-acetoxy (or benzoyloxy)ethylidenecyclohexanes by the catalysis of bis(acetonitrile)palladium(II) chloride.A mechanism related to the stereoselectivity and reactivity is discussed in terms of the conformational requirements in a transition state.

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