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927-82-2

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927-82-2 Usage

Chemical compound

2-amino-2-methylpropyl hydrogen sulfate

Physical properties

white crystalline solid, strong acidic taste, soluble in water

Uses

intermediate in pharmaceutical and agrochemical production, catalyst in organic synthesis, reagent in chemical analysis

Safety information

strong irritant to eyes, skin, and respiratory system, handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 927-82-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 927-82:
(5*9)+(4*2)+(3*7)+(2*8)+(1*2)=92
92 % 10 = 2
So 927-82-2 is a valid CAS Registry Number.

927-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-2-methylpropyl) hydrogen sulfate

1.2 Other means of identification

Product number -
Other names 2-amino-2-methylpropyl hydrogen sulfate

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:927-82-2 SDS

927-82-2Relevant articles and documents

(R)-2- Aryl -4,5-dihydrothiazole -4- carboxylic acid derivative as well as preparation method and application thereof (by machine translation)

-

Paragraph 0032; 0036; 0037, (2020/05/09)

The invention relates to (I - III) aryl - 4444, dihydrothiazoli- 4 4-carboxylic acid derivatives with bactericidal activity as shown in the general formula (R)- 2 - and a preparation method and application, of the pesticide molecular design method, throug

Efficient Direct Synthesis of Aziridine-Containing Chiral Tridentate Ligands by the Iminium-Mediated Self-Ring Opening Reaction of Enantiopure Aziridines and Salicylaldehydes

Chen, Xingpeng,Lin, Chao,Du, Hongguang,Xu, Jiaxi

, p. 1647 - 1661 (2019/02/27)

An efficient method for the direct synthesis of aziridine-containing chiral tridentate ligands was developed from enantiopure aziridines and salicylaldehydes. The method achieved the regiospecific cleavage of more substituted C?N bonds of aziridines through an iminium-mediated self-ring opening reaction of aziridines with up to 95% yield and complete inversion of configuration. The (S)-2-alkylaziridine-derived tridentate ligands displayed excellent activity and stereoselectivity in the zinc trifluoromethanesulfonate-catalyzed asymmetric aldol reactions of acetone and aromatic aldehydes. (Figure presented.).

Ti-Catalyzed Radical Alkylation of Secondary and Tertiary Alkyl Chlorides Using Michael Acceptors

Wu, Xiangyu,Hao, Wei,Ye, Ke-Yin,Jiang, Binyang,Pombar, Gisselle,Song, Zhidong,Lin, Song

supporting information, p. 14836 - 14843 (2018/11/10)

Alkyl chlorides are common functional groups in synthetic organic chemistry. However, the engagement of unactivated alkyl chlorides, especially tertiary alkyl chlorides, in transition-metal-catalyzed C-C bond formation remains challenging. Herein, we describe the development of a TiIII-catalyzed radical addition of 2° and 3° alkyl chlorides to electron-deficient alkenes. Mechanistic data are consistent with inner-sphere activation of the C-Cl bond featuring TiIII-mediated Cl atom abstraction. Evidence suggests that the active TiIII catalyst is generated from the TiIV precursor in a Lewis-acid-assisted electron transfer process.

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