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420727

Sigma-Aldrich

Chloro(dimethylsulfide)gold(I)

Synonym(s):

(Dimethylsulfide)gold(I) chloride

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5 G
¥3,961.20

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Available to ship on2025年4月25日Details

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1 G
¥344.58
5 G
¥3,961.20

About This Item

Linear Formula:
(CH3)2SAuCl
CAS Number:
29892-37-3
Molecular Weight:
294.55
MDL number:
MFCD00192090
UNSPSC Code:
12161600
PubChem Substance ID:
24866348
NACRES:
NA.22

¥344.58

List Price¥1,148.62Save 70%

Available to ship on2025年4月25日Details

Request a Bulk Order

form

powder

Quality Level

100

reaction suitability

core: gold
reagent type: catalyst

SMILES string

Cl[Au].CSC

InChI

1S/C2H6S.Au.ClH/c1-3-2;;/h1-2H3;;1H/q;+1;/p-1

InChI key

YQALRAGCVWJXGB-UHFFFAOYSA-M

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Anti-IP3 Receptor 1 Antibody

Anti-INSP3R1 antibody produced in rabbit affinity isolated antibody

SAB4501593

Anti-INSP3R1 antibody produced in rabbit

Monoclonal Anti-ITPR1 antibody produced in mouse clone 2B6, purified immunoglobulin, buffered aqueous solution

WH0003708M1

Monoclonal Anti-ITPR1 antibody produced in mouse

Anti-IP3 Receptor 2 Antibody serum, Chemicon®

AB9074

Anti-IP3 Receptor 2 Antibody

Quality Level

100

Quality Level

-

Quality Level

100

Quality Level

100

antibody form

affinity purified immunoglobulin

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

antibody form

serum

biological source

rabbit

biological source

rabbit

biological source

mouse

biological source

rabbit

shipped in

wet ice

shipped in

wet ice

shipped in

dry ice

shipped in

wet ice

Gene Information

human ... ITPR1(3708)

Gene Information

human ... ITPR1(3708)

Gene Information

human ... ITPR1(3708)

Gene Information

human ... ITPR2(3709)

species reactivity

rat

species reactivity

rat, human, mouse

species reactivity

human

species reactivity

human, mouse

Application

Chloro(dimethylsulfide)gold(I) can be used to synthesize a gold(I)-catalyst that can effectively catalyze intermolecular [2+2] cycloaddition of terminal alkynes with substituted alkenes to form substituted cyclobutenes under mild reaction conditions.[1]
It can also be used to synthesize:
  • chloro(trimesitylphosphine)gold(I)[2]
  • gold(I) N-heterocyclic carbene (NHC) complexes[3]
  • bis(carbene)gold(I) complex of ferrocenyl complexes[4]
  • gold(I) acetylide complexes[5]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    0000308954
    0000308954
    MKCW1094
    MKCT5112
    MKCQ7155

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    Find documentation for the products that you have recently purchased in the Document Library.

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    Synthesis and anticancer properties of gold (I) and silver (I) N-heterocyclic carbene complexes
    Siciliano T J, et al.
    Journal of Organometallic Chemistry, 696(5), 1066-1071 (2011)
    Chloro (dimethyl sulfide) gold (I)
    Jones P G, et al.
    Acta Crystallographica Section C, Crystal Structure Communications, 44(12), 2089-2091 (1988)
    A cytotoxic bis (carbene) gold (I) complex of ferrocenyl complexes: synthesis and structural characterisation.
    Horvath U E, et al.
    New. J. Chem., 32(3), 533-539 (2008)
    Intermolecular [2+ 2] Cycloaddition of Alkynes with Alkenes Catalyzed by Gold (I)
    de Orbe M E, et al.
    Organic Syntheses, 93, 115-126 (2003)
    Liquid-crystalline (lsonitrile) gold (I) acetylide complexes.
    Kaharu T, et al.
    Journal of Materials Chemistry, 5(4), 687-692 (1995)

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